New CPSC Data Shows 60% of All Fireworks Injuries Occur Around July 4th; Firecrackers, Aerials, Homemade Explosives Cause Most Deaths, Injuries
WASHINGTON, D.C. – Today on the grounds of the National Mall, the U.S. Consumer Product Safety Commission (CPSC) issued its annual report of deaths and injuries involving legal and illegal fireworks for calendar year 2012. Fireworks can have a life-altering impact on consumers, including severe eye injuries, loss of limbs, and even death. CPSC works closely with U.S. Customs and Border Protection (CBP); the Bureau of Alcohol, Tobacco, Fireworks, and Explosives; the Department of Transportation; and the Department of Justice to enforce federal safety standards and raise awareness about the dangers of fireworks.
Last year, CPSC received reports of six men who were killed by professional-grade, homemade or banned firework devices. In addition, an estimated 8,700 consumers were treated in U.S. hospital emergency departments for fireworks-related injuries.
Between June 22, 2012 and July 22, 2012, more than 5,000 consumers were treated in hospital emergency rooms due to fireworks-related injuries. Sixty percent of all fireworks injuries occur during the 30 days surrounding the July 4 holiday. More than half of these reported injuries involved burns to the hands, head and face. About 1,000 reported injuries involved sparklers and bottle rockets, fireworks that are frequently and incorrectly considered safe for young children.
Follow-up investigations of incidents showed that most injuries were associated with malfunctioning fireworks or improper use. Malfunctioning fireworks often resulted in unexpected flight paths and dangerous debris. Improper use included igniting fireworks too close to someone, lighting fireworks in one’s hand and playing with lit or used fireworks. Most victims recovered from their injuries or were expected to recover completely; however, several victims reported that their injuries might be long term.
“These figures represent more than numbers; they represent the lives of real people who have been affected well beyond the Fourth of July” said CPSC Chairman Inez Tenenbaum. “The federal government is working hard to keep the public safe by monitoring the ports, the marketplace, and the transportation of fireworks. Now, we need consumers to do their part and celebrate safely.”
Working with CBP, CPSC conducts surveillance on imported fireworks. During 2012, the agencies collected and tested shipments of imported fireworks for compliance with the Federal Hazardous Substance Act (FHSA). About 30 percent of the tested products were found to be in violation of the law and were immediately stopped at the U.S. port. This import surveillance program strives to keep violative and dangerous fireworks off of U.S. store shelves and roadside stands.
“The solid partnership between CBP, CPSC and other agencies at the Import Safety Commercial Targeting and Analysis Center (CTAC) enables greater sharing of information and targeting to ensure the safety of imported fireworks,” said CBP Assistant Commissioner Allen Gina. “Interagency collaboration at the CTAC results in the identification and interdiction of potentially unsafe imported merchandise, including non-compliant fireworks, and truly exemplifies working together as one U.S. Government at the Border to protect American consumers.”
At the national level, CBP, CPSC and the Pipeline Hazardous Materials Safety Administration (PHMSA) work side-by-side at the CTAC in Washington, DC to effectively combat the importation of illegal fireworks. The CTAC provides a platform for the agencies to share data, analyze import trends and conduct joint risk-based targeting to identify fireworks shipments that pose a safety risk.
“Fireworks are explosives. Protecting the public means making sure that our safety regulations work when these explosives are being transported,” said PHMSA Administrator Cynthia Quarterman.
“As the federal law enforcement agency charged with enforcing federal explosives laws, ATF actively works with other federal agencies, such as CPSC, through its fireworks enforcement program to protect the public from the dangers of illegal explosives devices,” said ATF Acting Director B. Todd Jones.
Consumers who decide to purchase legal fireworks are urged to take these safety steps.
Make sure the fireworks you want to buy are legal in your area before buying or using them.
Never allow young children to play with or ignite fireworks, including sparklers. Parents may not realize that young children suffer injuries from sparklers. Sparklers burn at temperatures of about 2,000 degrees ─ hot enough to melt some metals.
Always have an adult closely supervise fireworks activities if older children are allowed to handle devices.
Avoid buying fireworks that are packaged in brown paper because this is often a sign that the fireworks were made for professional displays and could pose a danger to consumers.
Never place any part of your body directly over a fireworks device when lighting the fuse. Back up to a safe distance immediately after lighting fireworks.
Keep a bucket of water or a garden hose handy in case of fire or other mishap.
Never try to relight or handle malfunctioning fireworks. Soak them with water and throw them away.
Never point or throw fireworks at another person.
Light fireworks one at a time, then move back quickly.
Never carry fireworks in a pocket or shoot them off in metal or glass containers.
After fireworks complete their burning, douse the spent device with plenty of water from a bucket or hose before discarding the device to prevent a trash fire.
ATF encourages the public to report the manufacture or sale of illegal fireworks to your local law enforcement agencies or to the ATF hotline at 1-888-ATF-BOMB (1-888-283-2662).
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Wednesday, June 26, 2013
Strollers Recalled by Kolcraft Due to Projectile Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: JUNE 19, 2013Recall number: 13-221
Recall Summary
Name of product:
Jeep Liberty Strollers
Hazard:
The inner tube of the tire on the stroller can rupture causing the wheel rim to fracture and fly off as a projectile, posing a risk of bodily injury and property damage.
Remedy:
View DetailsRepairConsumer Contact:
Kolcraft at (800) 453-7673 from 8 a.m. to 5 p.m. ET Monday through Friday or online at www.Kolcraft.com then click Safety Notifications for more information.
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Recall date: JUNE 19, 2013Recall number: 13-221
Recall Summary
Name of product:
Jeep Liberty Strollers
Hazard:
The inner tube of the tire on the stroller can rupture causing the wheel rim to fracture and fly off as a projectile, posing a risk of bodily injury and property damage.
Remedy:
View DetailsRepairConsumer Contact:
Kolcraft at (800) 453-7673 from 8 a.m. to 5 p.m. ET Monday through Friday or online at www.Kolcraft.com then click Safety Notifications for more information.
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Tuesday, June 25, 2013
Axis Arrows Recalled by Easton Due to Injury Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: JUNE 19, 2013Recall number: 13-220
Recall Summary
Name of product:
Easton Axis arrows
Hazard:
The arrows can break when fired and hit unintended targets, including the user and bystanders.
Remedy:
View DetailsReplaceConsumer Contact:
Easton Technical Products; toll-free at (888) 380-6234 from 8 a.m. to 8 p.m. ET Monday through Friday or online at www.eastonarchery.com and click on Axis Recall for more information or go to www.axisrecall.com.
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Recall date: JUNE 19, 2013Recall number: 13-220
Recall Summary
Name of product:
Easton Axis arrows
Hazard:
The arrows can break when fired and hit unintended targets, including the user and bystanders.
Remedy:
View DetailsReplaceConsumer Contact:
Easton Technical Products; toll-free at (888) 380-6234 from 8 a.m. to 8 p.m. ET Monday through Friday or online at www.eastonarchery.com and click on Axis Recall for more information or go to www.axisrecall.com.
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Ross Stores Agrees to $3.9 Million Civil Penalty
Ross Stores Agrees to $3.9 Million Civil Penalty, Internal Compliance Improvements for Failure to Report Drawstrings in Children’s Upper Outerwear
JUNE 21, 2013 Release Number: 13-224
WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission (CPSC) announced today that Ross Stores Inc., of Pleasanton, Calif., has agreed to pay a $3.9 million civil penalty. The penalty agreement has been accepted provisionally by the Commission in a 3-0 vote.
The settlement resolves CPSC staff’s charges that from January 2009 to February 2012, Ross knowingly failed to report to CPSC immediately, as required by federal law, that it sold or held for sale, about 23,000 children’s upper outerwear garments with drawstrings at the neck or waist. In February 1996, CPSC issued guidelines (which were incorporated into a consensus industry voluntary standard in 1997) to help prevent children from strangling or getting entangled on neck and waist drawstrings in upper garments, such as sweatshirts and jackets.
In May 2006, the Commission posted a letter on its website which stated that staff considered children’s upper outerwear with drawstrings at the hood or neck to be defective and present a substantial risk of injury to young children. In July 2011, based on the 1996 CPSC guidelines and the 1997 voluntary standard, CPSC issued a final rule which designates the hazards presented by drawstrings in children’s upper outerwear as substantial product hazards.
Ross’s distribution of some children’s garments occurred during the same period of time as CPSC’s investigation and negotiation of a 2009 civil penalty. The $500,000 penalty that Ross paid in 2009 was to settle staff charges that it failed to report four series of children’s upper outerwear drawstring garments distributed between 2006 and 2008. Ross’s distribution of the other garments in this matter occurred either partially or entirely after the effective date of CPSC’s Final Rule. There have been no reported injuries associated with the recalled garments.
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JUNE 21, 2013 Release Number: 13-224
WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission (CPSC) announced today that Ross Stores Inc., of Pleasanton, Calif., has agreed to pay a $3.9 million civil penalty. The penalty agreement has been accepted provisionally by the Commission in a 3-0 vote.
The settlement resolves CPSC staff’s charges that from January 2009 to February 2012, Ross knowingly failed to report to CPSC immediately, as required by federal law, that it sold or held for sale, about 23,000 children’s upper outerwear garments with drawstrings at the neck or waist. In February 1996, CPSC issued guidelines (which were incorporated into a consensus industry voluntary standard in 1997) to help prevent children from strangling or getting entangled on neck and waist drawstrings in upper garments, such as sweatshirts and jackets.
In May 2006, the Commission posted a letter on its website which stated that staff considered children’s upper outerwear with drawstrings at the hood or neck to be defective and present a substantial risk of injury to young children. In July 2011, based on the 1996 CPSC guidelines and the 1997 voluntary standard, CPSC issued a final rule which designates the hazards presented by drawstrings in children’s upper outerwear as substantial product hazards.
Ross’s distribution of some children’s garments occurred during the same period of time as CPSC’s investigation and negotiation of a 2009 civil penalty. The $500,000 penalty that Ross paid in 2009 was to settle staff charges that it failed to report four series of children’s upper outerwear drawstring garments distributed between 2006 and 2008. Ross’s distribution of the other garments in this matter occurred either partially or entirely after the effective date of CPSC’s Final Rule. There have been no reported injuries associated with the recalled garments.
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Tuesday, June 18, 2013
$3.5 million Settlement: Fetal heart monitor tracings at issue in birth trauma lawsuit
Plaintiff says a C-section should have taken place earlier; case is settled
In a medical malpractice/birth trauma lawsuit, plaintiff asserted that defendants failed to timely deliver the minor plaintiff in the face of abnormal findings on the electronic fetal heart monitor.
This delay was alleged to have resulted in a prolonged hypoxic-ischemic episode, which caused brain injury to the minor plaintiff. Manifestations of this brain injury include significant mental and motor delays, all of which are permanent.
At issue were the fetal heart monitor tracings that began to demonstrate deteriorating fetal condition, for which plaintiff argued there was not a timely response by the obstetrical staff.
Type of action: Medical malpractice, birth trauma
Type of injuries: Brain damage
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In a medical malpractice/birth trauma lawsuit, plaintiff asserted that defendants failed to timely deliver the minor plaintiff in the face of abnormal findings on the electronic fetal heart monitor.
This delay was alleged to have resulted in a prolonged hypoxic-ischemic episode, which caused brain injury to the minor plaintiff. Manifestations of this brain injury include significant mental and motor delays, all of which are permanent.
At issue were the fetal heart monitor tracings that began to demonstrate deteriorating fetal condition, for which plaintiff argued there was not a timely response by the obstetrical staff.
Type of action: Medical malpractice, birth trauma
Type of injuries: Brain damage
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BeBeLove Recalls Baby Bath Seats Due to Drowning Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: JUNE 18, 2013 Recall number: 13-217
Recall Summary
Name of product:
Baby Bath Seats
Hazard:
The bath seats fail to meet federal safety standards, including the requirements for stability. Specifically, the bath seats can tip over, posing a risk of drowning to babies.
Remedy:
View DetailsRefundConsumer Contact:
BeBeLove, toll-free at (888) 464-1218, from 9 a.m. to 5 p.m. PT Monday through Friday, or visit the firm’s website at www.bebeloveusa.com and click on the Recall Contact tab at the top of the page for more information.
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Recall date: JUNE 18, 2013 Recall number: 13-217
Recall Summary
Name of product:
Baby Bath Seats
Hazard:
The bath seats fail to meet federal safety standards, including the requirements for stability. Specifically, the bath seats can tip over, posing a risk of drowning to babies.
Remedy:
View DetailsRefundConsumer Contact:
BeBeLove, toll-free at (888) 464-1218, from 9 a.m. to 5 p.m. PT Monday through Friday, or visit the firm’s website at www.bebeloveusa.com and click on the Recall Contact tab at the top of the page for more information.
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Monday, June 17, 2013
Nine Innings of Brain Safety in Baseball
Clcik to view/download/print the tips to protect your kids.
Nine Innings of Brain Safety in Baseball from the CPSC
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Nine Innings of Brain Safety in Baseball from the CPSC
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Texsport Recalls Cedar Lake Heater/Cookers Due to Fire Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: JUNE 13, 2013 Recall number: 13-214
Recall Summary
Name of product:
Cedar Lake Propane Heater/Cooker
Hazard:
The regulator on the heater/cooker malfunctions when a user switches from a cooking to heating option, or vice versa, the gas propane turns to liquid, which can flare easily and pose a fire hazard.
Remedy:
View DetailsRefundConsumer Contact:
Texsport at (800) 231-1402 from 8 a.m. to 5 p.m. CT Monday through Friday or online at www.texsport.com and click on RECALL link.
From the CPSC
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Friday, June 14, 2013
Driver alert: Metro Detroit's most crash-prone intersections
Tom Greenwood, The Detroit News (Click to read)
The Ford and Haggerty roads intersection in Canton Township is the most crash prone in southeastern Michigan, edging out 11 Mile and Southfield Road.
According to the South East Michigan Council of Governments’ list of the 21st worst sites, Ford and Haggerty has averaged 67 crashes annually between 2008 and 2012 for a total of 335. The intersection is near the Metro area’s only IKEA store, numerous other businesses and close to a busy freeway.
The 11 Mile and Southfield Road intersection in Southfield placed second, averaging 65.8 annually for a five-year total of 329 crashes.
Longtime Southfield resident Jim Whiteford said he is extra cautious when driving on Southfield.
“The intersection at 10 Mile is bad, 11 Mile is really bad and 12 Mile is the worst,” Whiteford said. “You really have to pay attention because so many people blow the red lights at those intersections. I saw it happen the other day.”
Two other Southfield intersections made SEMCOG’s list: 10 Mile and Southfield is 17th worst, and Southfield and 12 Mile is 21st worst.
For Whiteford, two mitigating factors to the problem are the nearness of Interstate 696 and the way the intersections were built.
“The intersections are landlocked so they can’t do too much to rebuild them,” Whiteford said. “I live close to Southfield Road, close enough that I can hear the screeching tires and then the impact. When I hear that, I automatically call the police.”
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The Ford and Haggerty roads intersection in Canton Township is the most crash prone in southeastern Michigan, edging out 11 Mile and Southfield Road.
According to the South East Michigan Council of Governments’ list of the 21st worst sites, Ford and Haggerty has averaged 67 crashes annually between 2008 and 2012 for a total of 335. The intersection is near the Metro area’s only IKEA store, numerous other businesses and close to a busy freeway.
The 11 Mile and Southfield Road intersection in Southfield placed second, averaging 65.8 annually for a five-year total of 329 crashes.
Longtime Southfield resident Jim Whiteford said he is extra cautious when driving on Southfield.
“The intersection at 10 Mile is bad, 11 Mile is really bad and 12 Mile is the worst,” Whiteford said. “You really have to pay attention because so many people blow the red lights at those intersections. I saw it happen the other day.”
Two other Southfield intersections made SEMCOG’s list: 10 Mile and Southfield is 17th worst, and Southfield and 12 Mile is 21st worst.
For Whiteford, two mitigating factors to the problem are the nearness of Interstate 696 and the way the intersections were built.
“The intersections are landlocked so they can’t do too much to rebuild them,” Whiteford said. “I live close to Southfield Road, close enough that I can hear the screeching tires and then the impact. When I hear that, I automatically call the police.”
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Stride Rite Recalls Girl’s Sandals Due to Choking Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: JUNE 13, 2013 Recall number: 13-215
Recall Summary
Name of product:
“Joanna” Girl’s Sandal
Hazard:
The metal flower on the shoe can detach, posing a choking hazard.
Remedy:
View DetailsRefundConsumer Contact:
Stride Rite at (800) 365-4933, from 8 a.m. to 5 p.m. ET Monday through Friday, online at www.striderite.com and click on Product Safety Information under Customer Service for more information or e-mail JoannaReturns@striderite.com.
From the CPSC
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Recall date: JUNE 13, 2013 Recall number: 13-215
Recall Summary
Name of product:
“Joanna” Girl’s Sandal
Hazard:
The metal flower on the shoe can detach, posing a choking hazard.
Remedy:
View DetailsRefundConsumer Contact:
Stride Rite at (800) 365-4933, from 8 a.m. to 5 p.m. ET Monday through Friday, online at www.striderite.com and click on Product Safety Information under Customer Service for more information or e-mail JoannaReturns@striderite.com.
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Thursday, June 13, 2013
Symbios Medical Products Issues Nationwide Recall of GOPump and GOBlock Kits
FOR IMMEDIATE RELEASE - May 10, 2013 - Symbios Medical Products initiated a voluntary recall of all GoPump Rapid Recovery System kits and GOBlock Kits manufactured with flow control components assembled prior to July 2012. These products have been found to potentially cause excessively high flow rates, which presents a risk of patient toxicity and serious injury (e.g., seizure, dysrhythmia, death) due to the rapid influx of medication particularly in patients with low body mass or advanced age. To date, there have been 5 complaints received, 2 of which involved serious consequences. There have been no patient deaths reported. The root cause is understood and processes have been put in place to address the issue.
This recall affects only the fifty (50) United States plus the District of Columbia. Distributors and clinical provider sites using these Symbios Medical Products have been notified of the affected product codes and lot numbers. Symbios is working to secure all affected product and have it returned. Products subject to this recall were distributed between April 1st, 2011 and April 30th, 2013. Recall action was begun immediately upon the knowledge of the product related issues.
GOPUMP / GOBLOCK KITS SUBJECT TO RECALL
| Range of Affected Kit Lot #'s | |||
|---|---|---|---|
| Kit PN | From Kit Lot # | To Kit Lot # | Kit description |
| 510042 | 11-100251 | 13-100128 | GoPump kit 150mL, 2 mL/hr Epidural Catheter |
| 510042-BP | 12-101300 | 12-101300 | GoPump kit 150mL, 2 mL/hr, Epidural Catheter & BIOPATCH |
| 510080-BP | 11-100215 | 12-100508 | GoPump kit 300mL, 2 mL/hr/side, 5" Fenestrated Catheter and Biopatch |
| 510110 | 11-100664 | 11-100664 | GoPump kit 150mL, 2 mL/hr 2.5" Fenestrated Catheter |
| 510110-BP | 11-100838 | 12-101560 | GoPump kit 150mL, 2 mL/hr 2.5" Fenestrated Catheter and Biopatch |
| 510112-BP | 11-100839 | 13-100225 | GoPump kit 300mL, 2 mL/hr/side, 2.5" Fenestrated Catheter & BIOPATCH |
| 510141-BP | 12-100460 | 12-100673 | GoPump kit 300mL, 2 mL/hr/side, 10" Fenestrated Catheter & BIOPATCH |
| 510201-BP | 12-100108 | 12-101538 | GoPump kit 300mL, 2 ml/hr, 5" Fenestrated Catheter & BIOPATCH |
| 510203-BP | 12-101301 | 13-100611 | GoPump kit 300ml, 4 ml/hr, Epidural Cath & BIOPATCH |
| 510204 | 11-100505 | 11-100665 | GoPump kit 300ml, 4 ml/hr, 2.5" Fenestrated Cath |
| 510204-BP | 11-100721 | 13-100680 | GoPump kit 300ml, 4 ml/hr, 2.5" Fenestrated Cath & BIOPATCH |
| 510205-BP | 11-100722 | 13-100087 | GoPump kit 300ml, 4 ml/hr, 5" Fenestrated Catheter & BIOPATCH |
| 510349-BP | 12-100935 | 12-100935 | GoPump kit 300ml, 2 ml/hr, Epidural Catheter, 2.75" Needle, BIOPATCH |
| 510350 | 11-100353 | 12-100233 | GoPump kit 150ml, 2 ml/hr, Epidural Catheter, 2.75" Needle |
| 510350-BP | 12-100429 | 13-100047 | GoPump kit 150ml, 2 ml/hr, Epidural Catheter, 2.75" Needle, BIOPATCH |
| 510401-BP | 12-101045 | 12-101540 | GoPump kit 300mL, 2 mL/hr/side, 7.5" Catheters, BIOPATCH |
| 510458 | 11-100618 | 13-100703 | GOBlock Kit 600 ml, 10 ml/hr |
| 510462-BP | 11-100694 | 13-100092 | GoPump kit 600mL, 2 mL/hr/side, 5" Catheter, BIOPATCH |
| 510472 | 11-100385 | 13-100354 | GOBlock Kit 600 ml, 8 ml/hr |
| 510491 | 11-100601 | 13-100705 | GOBlock Kit 600 ml, 6 ml/hr |
| 510545-BP | 11-100718 | 13-100229 | GoPump kit 300mL, 2 mL/hr/side, 5" Fenestrated Catheter, BIOPATCH |
| 510551-BP | 11-100500 | 13-100672 | GoPump kit 300mL, 4 ml/hr, 2.5" Catheter, 2.75" Needle, BIOPATCH |
| 510556-BP | 11-100779 | 12-101552 | GoPump kit 150ml, 2 ml/hr, 2.5" Catheter with 2.75" Needle, BIOPATCH |
| 510558-BP | 12-100403 | 12-101343 | GoPump kit 600mL, 2 mL/hr/side, 10" Catheter, 6" needle, BIOPATCH |
| 510608 | 11-100695 | 12-101544 | GOBlock kit 300mL, 4 ml/hr |
| 510611 | 11-100302 | 13-100227 | GOBlock Kit 300ml, 4 ml/hr |
| 510612 | 11-100817 | 12-101475 | GOBlock Kit 300ml, 6 ml/hr |
| 510642 | 12-100616 | 13-100590 | GoPump kit 300mL, 2 ml/hr |
| 510643 | 12-100332 | 13-100183 | GoPump kit 600mL, 2 mL/hr/side |
| 510646 | 11-100632 | 12-101233 | GoPump kit 600mL, SF |
| 510644 | 11-100565 | 13-100169 | GoPump kit 300mL, 2 ml/hr per side |
| 510654 | 11-100833 | 13-100174 | GOPump kit 150mL, 2 ml/hr |
Consumers or using customer sites with questions may contact the company via telephone at 317-225-4447 ext 25 between the hours of 8:00am and 4:00pm.EST. Customers may also contact the company via e-mail at jcarty@symbiosmedical.com.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA:
- Online at http://www.fda.gov/MedWatch/report.htm
- http://www.fda.gov/MedWatch/getforms.htm
(form available to fax or mail), or - Call FDA 1-800-FDA-1088
Symbios Medical Products is committed to the highest level of product quality and fully regrets the most recent product related issues. The Board of Directors of Symbios and its Management Team are constantly reviewing our programs and processes for product requirements and quality of our product in support of pain control of our customer’s patients. The expanse of this action is indicative of our desire to insure safe and effective product availability.
Symbios Medical Products
7301 Georgetown Road Suite 150
Indianapolis, Indiana 46268 317‐225‐4447 Ext 25
www.symbiosmedical.com
7301 Georgetown Road Suite 150
Indianapolis, Indiana 46268 317‐225‐4447 Ext 25
www.symbiosmedical.com
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Philips Recalls Metal Halide Lamps Due to Fire, Laceration Hazards
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: JUNE 06, 2013 Recall number: 13-211
Recall Summary
Name of product:
Metal Halide Lamps
Hazard:
The internal wiring can arc causing the lamp to catch fire or the glass to shatter. This poses fire and laceration hazards.
Remedy:
View DetailsRefundReplaceConsumer Contact:
Philips Lighting Company at (800) 372-3331, from 7 a.m. to 5 p.m. CT Monday through Friday, at e-mail qualityadvisory2013@philips.com, or online at www.philips.com/recall for more information.
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Recall date: JUNE 06, 2013 Recall number: 13-211
Recall Summary
Name of product:
Metal Halide Lamps
Hazard:
The internal wiring can arc causing the lamp to catch fire or the glass to shatter. This poses fire and laceration hazards.
Remedy:
View DetailsRefundReplaceConsumer Contact:
Philips Lighting Company at (800) 372-3331, from 7 a.m. to 5 p.m. CT Monday through Friday, at e-mail qualityadvisory2013@philips.com, or online at www.philips.com/recall for more information.
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Wednesday, June 12, 2013
Townsend Farms Voluntarily Recalls Limited Lots of Frozen Organic Antioxidant Blend Products Due To Possible Health Risk
UPDATED RELEASE #2 Harris Teeter Lot Code and Best By Correction Townsend Farms Voluntarily Recalls Limited Lots of Frozen Organic Antioxidant Blend Products Due To Possible Health Risk
Contact:
Consumer:
(800) 875-5291
townsendfarms5148@stericycle.com
FOR IMMEDIATE RELEASE - June 4, 2013 - Townsend Farms, Inc. of Fairview, Oregon, has announced that it is voluntarily recalling certain lots of its frozen Organic Antioxidant Blend, out of an abundance of caution, because it has the potential to be contaminated with Hepatitis A virus, based on an ongoing epidemiological and traceback investigation by the FDA and the CDC of an illness outbreak. No other Townsend Farms products, frozen or fresh, are covered by this voluntary recall or linked to the illness outbreak at this time. This release confirms the correct Lot codes for Harris Teeter Products.
The product was sold at Costco warehouse stores under the product name Townsend Farms Organic Antioxidant Blend, 3 lb. bag and UPC 0 78414 404448. The recalled codes are located on the back of the package with the words "BEST BY"; followed by the code T012415 sequentially through T053115, followed by a letter. All of these letter designations are included in this recall for the lot codes listed above. Photos of the package are attached.
The product was also sold at Harris Teeter stores from April 19 until May 7, 2013, under the product name Harris Teeter Organic Antioxidant Berry Blend, 10 oz. bag UPC 0 72036 70463 4. The correct "Lot" and "best by" codes are as follows: Lot Codes T041613E, T041613C and a "BEST BY" code of 101614. Photos of the packaging are attached.
Townsend Farms is implementing this voluntary recall after learning that one of the ingredients of the frozen Organic Antioxidant Blend, pomegranate seeds processed in Turkey, may be linked to an illness outbreak outside of the United States. Thirty-four cases of Hepatitis A are being investigated to date in the U.S.; all are recovering. At this time, Hepatitis A has not been found in the product, but Townsend Farms is taking this precautionary action in consultation with the FDA, as the investigation continues.
Hepatitis A is a contagious liver disease that results from exposure to the Hepatitis A virus, including from food. It can range from a mild illness lasting a few weeks to a serious illness lasting several months. Illness generally occurs within 15 to 50 days of exposure and includes fatigue, abdominal pain, jaundice, abnormal liver tests, dark urine and pale stool. Hepatitis A vaccination can prevent illness if given within two weeks of exposure to a contaminated food. In rare cases, particularly consumers who have a pre- existing severe illness or are immune compromised, Hepatitis A infection can progress to liver failure.
Persons who may have consumed affected product should consult with their health care professional or local health department to determine if a vaccination is appropriate, and consumers with symptoms of Hepatitis A should contact their health care professionals or the local health department immediately. Consumers with the product should not consume the product. The product should be disposed of immediately. Please keep proof of product purchase.
TOWNSEND FARMS INC. is committed to producing the highest quality products, and is a certified Safety Quality Food facility. Townsend Farms, Inc. follows industry Good Manufacturing Practices (GMP) and sanitation procedures to ensure that its food products are safely handled and processed.
For questions or more information, contact a Townsend Farms Customer Service Representative by phone or e-mail at 1-800-875-5291; townsendfarms5148@stericycle.com.
Customer service representatives will be available Monday through Friday, 8 a.m. to 8 p.m. PDT to respond to inquiries.
Thank you so much from The Townsend Farm Family.
Mike Townsend, President Townsend Farms, Inc.
Margaret Townsend, Vice President Townsend Farms, Inc.
From the FDA
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Contact:
Consumer:
(800) 875-5291
townsendfarms5148@stericycle.com
FOR IMMEDIATE RELEASE - June 4, 2013 - Townsend Farms, Inc. of Fairview, Oregon, has announced that it is voluntarily recalling certain lots of its frozen Organic Antioxidant Blend, out of an abundance of caution, because it has the potential to be contaminated with Hepatitis A virus, based on an ongoing epidemiological and traceback investigation by the FDA and the CDC of an illness outbreak. No other Townsend Farms products, frozen or fresh, are covered by this voluntary recall or linked to the illness outbreak at this time. This release confirms the correct Lot codes for Harris Teeter Products.
The product was sold at Costco warehouse stores under the product name Townsend Farms Organic Antioxidant Blend, 3 lb. bag and UPC 0 78414 404448. The recalled codes are located on the back of the package with the words "BEST BY"; followed by the code T012415 sequentially through T053115, followed by a letter. All of these letter designations are included in this recall for the lot codes listed above. Photos of the package are attached.
The product was also sold at Harris Teeter stores from April 19 until May 7, 2013, under the product name Harris Teeter Organic Antioxidant Berry Blend, 10 oz. bag UPC 0 72036 70463 4. The correct "Lot" and "best by" codes are as follows: Lot Codes T041613E, T041613C and a "BEST BY" code of 101614. Photos of the packaging are attached.
Townsend Farms is implementing this voluntary recall after learning that one of the ingredients of the frozen Organic Antioxidant Blend, pomegranate seeds processed in Turkey, may be linked to an illness outbreak outside of the United States. Thirty-four cases of Hepatitis A are being investigated to date in the U.S.; all are recovering. At this time, Hepatitis A has not been found in the product, but Townsend Farms is taking this precautionary action in consultation with the FDA, as the investigation continues.
Hepatitis A is a contagious liver disease that results from exposure to the Hepatitis A virus, including from food. It can range from a mild illness lasting a few weeks to a serious illness lasting several months. Illness generally occurs within 15 to 50 days of exposure and includes fatigue, abdominal pain, jaundice, abnormal liver tests, dark urine and pale stool. Hepatitis A vaccination can prevent illness if given within two weeks of exposure to a contaminated food. In rare cases, particularly consumers who have a pre- existing severe illness or are immune compromised, Hepatitis A infection can progress to liver failure.
Persons who may have consumed affected product should consult with their health care professional or local health department to determine if a vaccination is appropriate, and consumers with symptoms of Hepatitis A should contact their health care professionals or the local health department immediately. Consumers with the product should not consume the product. The product should be disposed of immediately. Please keep proof of product purchase.
TOWNSEND FARMS INC. is committed to producing the highest quality products, and is a certified Safety Quality Food facility. Townsend Farms, Inc. follows industry Good Manufacturing Practices (GMP) and sanitation procedures to ensure that its food products are safely handled and processed.
For questions or more information, contact a Townsend Farms Customer Service Representative by phone or e-mail at 1-800-875-5291; townsendfarms5148@stericycle.com.
Customer service representatives will be available Monday through Friday, 8 a.m. to 8 p.m. PDT to respond to inquiries.
Thank you so much from The Townsend Farm Family.
Mike Townsend, President Townsend Farms, Inc.
Margaret Townsend, Vice President Townsend Farms, Inc.
From the FDA
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Voluntary Recall of Weight Loss Pills “Bethel 30” Found to Contain an Undeclared Drug Ingredient
Bethel Nutritional Consulting, Inc. Issues a Voluntary Recall of Weight Loss Pills “Bethel 30” Found to Contain an Undeclared Drug Ingredient
Contact Consumer:
212-568-5330
customerservice@bethel30.com
FOR IMMEDIATE RELEASE - June 11, 2013 - Bethel Nutritional Consulting, Inc. was informed by the Food and Drug Administration (FDA) that a sample of Bethel 30 green capsule was collected and tested by FDA in April 24, 2013. The capsules tested positive for Sibutramine and Phenolphthalein. Sibutramine is a controlled substance that was removed from the market in October 2010 for safety reasons. The FDA has not approved Bethel 30, green capsules as drugs; therefore the safety and effectiveness of this product is unknown.
FDA advises that these products may pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. This product may also interact, in life-threatening ways, with other medications a consumer may be taking.
Bethel 30, green capsules are marketed as a Natural Herb for Weight Loss manufactured with a pharmaceutical & Nutraceuticals laboratory. Bethel 30 Herb Supplement is packaged in plastic white bottles containing 30 capsules per bottle and bears Lot #’s 120514, with EXP: 12/05/2014.
The lot 120514 is the only one subject to recall and it will not be distributed through www.bethel30.com, or retail in office.
The product was sold directly to individual customers in our New York, NY, sales office and online at www.bethel30.com. The company discontinued total distribution. It sincerely regrets any inconvenience to our customers.
From the FDA
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Contact Consumer:
212-568-5330
customerservice@bethel30.com
FOR IMMEDIATE RELEASE - June 11, 2013 - Bethel Nutritional Consulting, Inc. was informed by the Food and Drug Administration (FDA) that a sample of Bethel 30 green capsule was collected and tested by FDA in April 24, 2013. The capsules tested positive for Sibutramine and Phenolphthalein. Sibutramine is a controlled substance that was removed from the market in October 2010 for safety reasons. The FDA has not approved Bethel 30, green capsules as drugs; therefore the safety and effectiveness of this product is unknown.
FDA advises that these products may pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. This product may also interact, in life-threatening ways, with other medications a consumer may be taking.
Bethel 30, green capsules are marketed as a Natural Herb for Weight Loss manufactured with a pharmaceutical & Nutraceuticals laboratory. Bethel 30 Herb Supplement is packaged in plastic white bottles containing 30 capsules per bottle and bears Lot #’s 120514, with EXP: 12/05/2014.
The lot 120514 is the only one subject to recall and it will not be distributed through www.bethel30.com, or retail in office.
The product was sold directly to individual customers in our New York, NY, sales office and online at www.bethel30.com. The company discontinued total distribution. It sincerely regrets any inconvenience to our customers.
From the FDA
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Gerber Recalls Machetes with Stitched Sheaths Due to Laceration Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: JUNE 06, 2013 Recall number: 13-209
Recall Summary
Name of product:
Gerber® Bear Grylls Parang Machete with stitched sheaths
Hazard:
The Parang machete can cut through the stitching of the sheaths when the blade is taken from or replaced in the sheath, posing a laceration hazard.
Remedy:
View DetailsReplaceConsumer Contact:
Gerber Legendary Blades toll-free at (877) 314-9130 from 9 a.m. to 5 p.m. PT Monday through Friday or online at www.gerbergear.com and click on “Product Notifications” at the bottom of the page.
From the CPSC
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Recall date: JUNE 06, 2013 Recall number: 13-209
Recall Summary
Name of product:
Gerber® Bear Grylls Parang Machete with stitched sheaths
Hazard:
The Parang machete can cut through the stitching of the sheaths when the blade is taken from or replaced in the sheath, posing a laceration hazard.
Remedy:
View DetailsReplaceConsumer Contact:
Gerber Legendary Blades toll-free at (877) 314-9130 from 9 a.m. to 5 p.m. PT Monday through Friday or online at www.gerbergear.com and click on “Product Notifications” at the bottom of the page.
From the CPSC
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Tuesday, June 11, 2013
Authorities cracking down on aggressive driving on I-75
While police are always on the lookout for aggressive drivers, they’ll be especially watchful Tuesday along a stretch of Interstate 75 in Oakland County.
From 10 a.m. until 2 p.m., members of the Southeast Oakland County Crash Investigation Team will zero-in on bad drivers in a special enforcement zone from Baldwin Road in Auburn Hills to 14 Mile in Troy.
The team of officers from Auburn Hills, Troy and Bloomfield Township will be watching for exhibitions of aggressive driving such as speeding, tailgating and improper lane changes.
The team was formed so that participating cities could share resources to investigate crashes that occur within their city/township limits. Since it was formed in 2010, the partnership reduces costs and has reduced the time it takes officers to clear crash sites.
The tab for Tuesday’s special enforcement effort is being underwritten by a $5,000 grant from the Michigan Association of Chiefs of Police.
Tom Greenwood
The Detroit News
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From 10 a.m. until 2 p.m., members of the Southeast Oakland County Crash Investigation Team will zero-in on bad drivers in a special enforcement zone from Baldwin Road in Auburn Hills to 14 Mile in Troy.
The team of officers from Auburn Hills, Troy and Bloomfield Township will be watching for exhibitions of aggressive driving such as speeding, tailgating and improper lane changes.
The team was formed so that participating cities could share resources to investigate crashes that occur within their city/township limits. Since it was formed in 2010, the partnership reduces costs and has reduced the time it takes officers to clear crash sites.
The tab for Tuesday’s special enforcement effort is being underwritten by a $5,000 grant from the Michigan Association of Chiefs of Police.
Tom Greenwood
The Detroit News
Do you know what to do if your in an accident? Download our guide for auto accident tips.
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IKEA Recalls LYDA Jumbo Coffee/Tea Cups Due to Burn Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: JUNE 06, 2013 Recall number: 13-210
Recall Summary
Name of product:
LYDA jumbo cups
Hazard:
The cups can break when hot liquid is poured into them, posing a burn hazard.
Remedy:
View DetailsRefundConsumer Contact:
IKEA, toll-free at (888) 966-4532 anytime or online at www.ikea-usa.com and click on the recall link on the home page.
From the CPSC
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Recall date: JUNE 06, 2013 Recall number: 13-210
Recall Summary
Name of product:
LYDA jumbo cups
Hazard:
The cups can break when hot liquid is poured into them, posing a burn hazard.
Remedy:
View DetailsRefundConsumer Contact:
IKEA, toll-free at (888) 966-4532 anytime or online at www.ikea-usa.com and click on the recall link on the home page.
From the CPSC
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Friday, June 7, 2013
DiveAlert Emergency Signaling Devices Recalled by Ideations Due to Drowning Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: JUNE 05, 2013 Recall number: 13-207
Recall Summary
Name of product:
DiveAlert and DiveAlert PLUS signaling devices
Hazard:
The signaling device can malfunction when used and restrict the diver’s air flow, posing a drowning hazard.
Remedy:
View DetailsRepairConsumer Contact:
DiveAlert, at (800) 275-4332 from 8 a.m. to 5 p.m. PT Monday through Friday, by e-mail at info@divealert.com or online at www.divealert.com and click on Recall for more information
Recall date: JUNE 05, 2013 Recall number: 13-207
Recall Summary
Name of product:
DiveAlert and DiveAlert PLUS signaling devices
Hazard:
The signaling device can malfunction when used and restrict the diver’s air flow, posing a drowning hazard.
Remedy:
View DetailsRepairConsumer Contact:
DiveAlert, at (800) 275-4332 from 8 a.m. to 5 p.m. PT Monday through Friday, by e-mail at info@divealert.com or online at www.divealert.com and click on Recall for more information
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Thursday, June 6, 2013
$450,000 Settlement: Woman injured after falling against door, down stairs
Owner claims door had a latch, but ex-employee testifies that it never did
Type of action: Premises liability
Types of injuries: Traumatic brain injury, post-traumatic seizure disorder, permanent cognitive difficulties, abnormal EEG, loss of smell and taste, memory loss
Name of case: Truett v. The Saline Tavern Inc.
Court/Case no./Date: Washtenaw County Circuit Court; 11-288-NO; Nov. 26, 2012
Type of action: Premises liability
Types of injuries: Traumatic brain injury, post-traumatic seizure disorder, permanent cognitive difficulties, abnormal EEG, loss of smell and taste, memory loss
Name of case: Truett v. The Saline Tavern Inc.
Court/Case no./Date: Washtenaw County Circuit Court; 11-288-NO; Nov. 26, 2012
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Pottery Barn Kids Recalls Sweet Lambie Crib Bumpers Due to Entanglement Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: MAY 29, 2013 Recall number: 13-204
Recall Summary
Name of product:
Sweet Lambie Crib Bumper
Hazard:
The thread in the decorative stitching on the bumper can loosen, posing an entanglement hazard to infants.
Remedy:
View DetailsRefundReplaceConsumer Contact:
Pottery Barn Kids; toll-free at (855) 323-5138, from 7 a.m. to midnight ET daily, or online at www.potterybarnkids.com and click on Safety Recalls at the bottom of the page for more information.
From the CPSC
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Recall date: MAY 29, 2013 Recall number: 13-204
Recall Summary
Name of product:
Sweet Lambie Crib Bumper
Hazard:
The thread in the decorative stitching on the bumper can loosen, posing an entanglement hazard to infants.
Remedy:
View DetailsRefundReplaceConsumer Contact:
Pottery Barn Kids; toll-free at (855) 323-5138, from 7 a.m. to midnight ET daily, or online at www.potterybarnkids.com and click on Safety Recalls at the bottom of the page for more information.
From the CPSC
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Wednesday, June 5, 2013
$250,000 Settlement: Worker asserts business owner harassed her
She argues an ongoing pay-for-sex relationship expected; case is settled
Types of actions: Quid pro quo discrimination and sexual harassment, assault and battery, tortious interference, ethnic intimidation
Types of injuries: Emotional distress, mental anguish, constructive discharge
Court/Case no./Date: Genesee County Circuit Court; 12-98423-NI; May 11, 2013
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Types of actions: Quid pro quo discrimination and sexual harassment, assault and battery, tortious interference, ethnic intimidation
Types of injuries: Emotional distress, mental anguish, constructive discharge
Court/Case no./Date: Genesee County Circuit Court; 12-98423-NI; May 11, 2013
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KTM North America Recalls KTM and Husaberg Motorcycles Due to Crash Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: MAY 29, 2013 Recall number: 13-203
Recall Summary
Name of product:
Competition/Closed Course and Enduro Motorcycles
Hazard:
During use, the throttle cable can malfunction and result in an uncontrollable throttle. This poses a crash hazard to the rider.
Remedy:
View DetailsRepairConsumer Contact:
KTM North America Inc. or Husaberg North America toll-free at (888) 985-6090 from 8 a.m. to 5 p.m. ET Monday through Friday, or online at www.ktm.com, then click on Dealer & Service and select Service, or at www.husaberg.com, click on Dealers & Service, then select Service, then click on Service & Safety Check for more information.
From the CPSC
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Click here for our motorcycle accident quick reference guide.
Recall date: MAY 29, 2013 Recall number: 13-203
Recall Summary
Name of product:
Competition/Closed Course and Enduro Motorcycles
Hazard:
During use, the throttle cable can malfunction and result in an uncontrollable throttle. This poses a crash hazard to the rider.
Remedy:
View DetailsRepairConsumer Contact:
KTM North America Inc. or Husaberg North America toll-free at (888) 985-6090 from 8 a.m. to 5 p.m. ET Monday through Friday, or online at www.ktm.com, then click on Dealer & Service and select Service, or at www.husaberg.com, click on Dealers & Service, then select Service, then click on Service & Safety Check for more information.
From the CPSC
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Click here for our motorcycle accident quick reference guide.
Monday, June 3, 2013
$9.5 million Verdict: Family of man who drowned saving boy seeks damages
Defendants should have foreseen children playing around area, plaintiffs say
Type of action: Negligence, wrongful death
Type of injuries: Death
Court/Case nos./Date: Wayne County Circuit Court; 09-028671-NO, 10-013593-NO; May 9, 2013
Tried before: Jury
Verdict amount: $9.5 million
Type of action: Negligence, wrongful death
Type of injuries: Death
Court/Case nos./Date: Wayne County Circuit Court; 09-028671-NO, 10-013593-NO; May 9, 2013
Tried before: Jury
Verdict amount: $9.5 million
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H&M Reannounces Recall of Children’s Water Bottles Due to Choking Hazard
Consumers should stop using this product unless otherwise instructed. It is illegal to resell or attempt to resell a recalled consumer product.
Recall date: MAY 29, 2013 Recall number: 13-201
Recall Summary
Name of product:
Children’s Water Bottles
Hazard:
The water bottle's spout can break off, posing a choking hazard to children.
Remedy:
View DetailsRefundConsumer Contact:
H&M toll-free at (855) 466-7467 from 7 a.m. to 12 midnight CT daily or visit the firm's website at www.hm.com and click on United States, then Customer Service at the bottom of the page and Recalled Items from the left column for more information.
From the CPSC
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Recall date: MAY 29, 2013 Recall number: 13-201
Recall Summary
Name of product:
Children’s Water Bottles
Hazard:
The water bottle's spout can break off, posing a choking hazard to children.
Remedy:
View DetailsRefundConsumer Contact:
H&M toll-free at (855) 466-7467 from 7 a.m. to 12 midnight CT daily or visit the firm's website at www.hm.com and click on United States, then Customer Service at the bottom of the page and Recalled Items from the left column for more information.
From the CPSC
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