US Recalls

Posted By Jim Vititoe on February 3, 2010

Company Contact:
Abdul Bakhtari
646-235-4154

FOR IMMEDIATE RELEASE – February 01, 2010 – Global Commodities Inc. of Hicksville, NY is recalling its 0.50 lbs. packages of Aahu Barah brand Dry Apricot food treats because they contain undeclared Sulfites. People who have allergies to Sulfites run the risk of serious or life-threatening allergic reaction if they consume this product.

The recalled Dry Apricots were distributed in New York State in some retail stores. The product comes in a 0.50 lbs., clear plastic package marked with Dry Apricot with an expiration date of 12/2013 stamped on the side.

No illnesses have been reported to date in connection with this problem.

The recall was initiated after routine sampling by NY State Agriculture & Markets inspectors and subsequent analysis by Food Laboratory personnel revealed the presence of sulfites in the 0.50 lbs. package of dried apricots which were not declared on the label. Subsequently, investigation indicated the problem was caused by a temporary breakdown in the company’s production and packaging processes. Production of the product has been suspended until the company is certain that the problem has been corrected.

The consumption of 10 mg of sulfites per serving has been reported to illicit severe reactions in some asthmatics.

Consumers who have purchased 0.50 lbs. packages of Aahu Barah brand “Dry Apricot” are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-516-396-0710 or 1-646-235-4154.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

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Posted By Jim Vititoe on February 3, 2010

FOR IMMEDIATE RELEASE
February 3, 2010
Release # 10-132 Firm’s Recall Hotline: (800) 678-9258
CPSC Recall Hotline: (800) 638-2772
CPSC Media Contact: (301) 504-7908
Dollar General Recalls Toy Guns Due to Choking Hazard

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Special Forces and Police SWAT Toy Gun Sets

Units: About 9,600

Retailer: Dollar General, of Goodlettsville, Tenn.

Importer: Dolgencorp LLC, of Goodlettsville, Tenn.

Hazard: The orange tips located at the end of the toy guns’ barrels, which are designed to distinguish them from real guns, can easily be removed from the barrels, posing a choking hazard to children.

Incidents/Injuries: None reported.

Description: This recall includes a Special Forces Weapons and Accessories Set and a SWAT Police Play Equipment Set. Each set includes two toy guns and related accessories. The number 48JQH09 is printed on the right side of the larger gun included in the recalled sets.

Sold at: Dollar General stores in 35 states from September 2009 through October 2009 for about $5.

Manufactured in: China

Remedy: Consumers should immediately take the recalled toy guns away from children and return them to any Dollar General for a full refund or a replacement product.

Consumer Contact: For additional information, contact Dollar General Corp. at (800) 678-9258 between 9 a.m. and 6 p.m. ET Monday through Friday, or visit the firm’s Web site at www.dollargeneral.com

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

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Posted By Jim Vititoe on February 3, 2010

FDA notified healthcare professionals of a Class I recall of the Aquarius Hemodialysis System, Model number GEF09800, because of reports of clinically significant fluid imbalance. When a certain level of fluid imbalance is detected, the Aquarius will trigger an alarm. However, users are able to override this alarm and continue therapy. It is possible to remove too much fluid from or replace too much fluid to the patient. In repeated cases, this imbalance increases, and may result in serious injuries or death. Baxter International, Inc. is the U.S. distributor of the Aquarius system.

The company notified its customers of a planned software upgrade to prevent users from bypassing the fluid balance alarm more than five times in a 20-minute period.

Edwards Lifesciences Inc., Aquarius Hemodialysis System
Recall Class: Class I
Product Name: Aquarius Hemodialysis System
Model Number: GEF09800
This product has been manufactured from June 2008 to the present.
Date Recall Initiated: March 16, 2009
Use:
A Hemodialysis system is used to clean waste products and extra fluid from the body after the kidneys have failed. It also monitors the amount of fluid going into and out of the patient.
Recalling Firm:
Edwards Lifesciences, LLC
1 Edwards Way
Irvine, California 92614-5688
Reason for Recall:
Edwards Lifesciences is conducting an Urgent Product Recall for the Aquarius Hemodialysis System because of reports of clinically significant fluid imbalance. When a certain level of fluid imbalance is detected, the Aquarius will trigger an alarm. However, users are able to override this alarm and continue therapy. It is possible to remove too much fluid from or replace too much fluid to the patient. In repeated cases, this imbalance increases, and may result in serious injuries or death.
Public Contact:
Baxter International, Inc. is the U.S. distributor of the Aquarius. For questions regarding the Aquarius, contact the Baxter Clinical Help Line at 1-888-736-2543.
FDA District: Los Angeles
FDA Comments:
On January 11, 2010, the company sent its customers an “Urgent Product Recall” letter. It included the:
description of the affected product, problem, and potential hazard
advice on action to be taken
revised device labeling
information concerning the planned software upgrade to prevent users from bypassing the fluid balance alarm more than five times in a 20-minute period
instruction to pass the notice on and inform all other employees within the company/organization that needed to be aware of the problem
instruction to transfer the notice to other organizations which
this action had an impact
other organizations may have received the potentially affected devices through a transfer
The “Urgent Product Recall” letter updates and expands the “Field Safety Notice” sent to customers on March 16, 2009.
Class 1 recalls are the most serious type of recall and involve situations in which there is a reasonable probability that use of these products will cause serious adverse health consequences or death.
Health care professionals and consumers may report adverse reactions or quality problems experienced with the use of these products to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail, or by FAX.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

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Posted By Jim Vititoe on February 3, 2010

FDA notified healthcare professionals of a Class I recall of Hettich Centrifuges with 2050 and 2076 plastic rotors, used in combination with the Mikro 12-24, Mikro 20, Haematokrit 20 and Haematokrit 24 bench top plastic centrifuges. The recall was initiated because the plastic centrifuge rotor may crack, break apart and be forcefully ejected through the plastic centrifuge housing at a high rate of speed. This may result in serious personal injury and damage to the surrounding area.

The device separates the red blood cells from plasma to determine the patient’s hematocrit. These recalled devices were distributed from January, 1999 through November, 2009. Hospitals, clinics and laboratories who have the listed centrifuge/rotor combination should immediately stop using the plastic rotors and contact Hettich to have these affected rotors replaced with metal rotors. The centrifuges can be identified by reading the model number on the front of the instrument or the name tag on the rear of the centrifuge; the rotors have the model numbers 2076 or 2050 stamped on them.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

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Posted By Jim Vititoe on February 3, 2010

Exel/Exelint Huber needles,
Exel/Exelint Huber Infusion Sets
Exel/Exelint “Securetouch+” Safety Huber Infusion Sets
Audience: Hospital Risk Managers, Surgical Service personnel
[Posted 01/26/2010] FDA notified healthcare professionals of a Class I recall of Exel/Exelint Huber needles, Exel/Exelint Huber Infusion Sets and Exel/Exelint “Securetouch+” Safety Huber Infusion Sets, manufactured by Nipro Medical Corporation for Exelint International Corporation. Huber needles are used to access ports implanted under the skin of chronically ill patients for repeated access to veins for the withdrawal of blood and infusion of medication, nutritional solutions, blood products, and imaging solutions.
The recall was initiated due to ‘coring’, the cutting or dislodging of silicone cores or slivers from the ports into which they are inserted. Coring may lead to decreased effectiveness of the port, infection, necrosis, swelling, embolization, or need for additional surgery to replace implanted port.
Inspections conducted in October 2009 of Nipro facilities found that their needles “cored” in 60 to 72 percent of tests. The reason for this coring is related to design and manufacturing processes, which the FDA continues to investigate and will update the public if there are new developments.
Hospitals, clinics and patients who have needles from these lists should immediately stop using these affected products and return any unused products to Exelint International Corporation.
There are more than 2 million units impacted by this recall in distribution nationwide. Recalled needles were manufactured from January 2007 to August 2009. Units subject to recall have a lot number that begins with “07,” “08,” “09,” and one of the product codes or catalog numbers noted in the FDA news release.
[01/26/2010 - Recall Notice - FDA]

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

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Posted By Jim Vititoe on February 3, 2010

FDA NEWS RELEASE

For Immediate Release: Jan. 26, 2010
Media Inquiries: Peper Long, 301-796-4671, mailto:mary.long@fda.hhs.gov
Consumer Inquiries: 888-INFO-FDA

The U.S. Food and Drug Administration today announced a Class I recall of Exel/Exelint Huber needles, Exel/Exelint Huber Infusion Sets and Exel/Exelint “Securetouch+” Safety Huber Infusion Sets, manufactured by Nipro Medical Corporation for Exelint International Corporation.
Huber needles are used to access ports implanted under the skin of chronically ill patients for repeated access to veins for the withdrawal of blood and infusion of medication, nutritional solutions, blood products, and imaging solutions. These needles should be designed to penetrate the port without cutting and dislodging any silicone cores (or slivers) from the ports into which they are inserted.

Inspections conducted in October 2009 of Nipro facilities in Japan found that their needles “cored” in 60 to 72 percent of tests. The reason for this coring is related to design and manufacturing processes, which the FDA continues to investigate.

There are more than 2 million units impacted by this recall in distribution nationwide. Recalled needles were manufactured from January 2007 to August 2009. Units subject to recall have a lot number that begins with “07,” “08,” “09,” and one of the following product codes or catalog numbers:

Exel/Exelint Huber Needles Product Codes/Catalog Numbers
26901
26902
26904
26906
26907
26908
26909
26911
26921
26922
26923
26924
26925
Exel/Exelint Huber Infusion Sets Product Codes/Catalog Numbers
With/Injection Site:
27940R
27941R
27944R
27945R
27946R
27948R
27949R
27950R

Without/Injection Site Product Codes/Catalog Numbers:
27954R
27955R
27958R
27959R

Exel/Exelint “SecureTouch +” Safety Huber Sets Product Codes/Catalog Numbers:
37854S
37855S
37858S

Hospitals, clinics and patients who have needles from these lists should immediately stop using these affected products and return any unused products to Exelint International Corporation. Direct all questions concerning this recall to:

Attn: Armand Hamid
EXEL International
5408 West Centinela Ave
Los Angeles, Calif. 90045-1504
Tel. 800-940-3935
Fax 800-308-5048
E-mail: info@exelint.com
Following hospital reports to the FDA of leakage after accessing the port with a Huber needle (labeled to be non-coring), the agency conducted it own laboratory testing of Huber needles from multiple manufacturers. This testing showed that certain Huber needles produced cores when inserted into ports. However, at this time only needles manufactured by Nipro have shown a high frequency for coring. The agency is continuing its investigation and will update the public if there are new developments.

At this time, the FDA has not received any adverse event reports related to silicone foreign bodies released in patients from Huber needle coring.The agency received only reports of port leakage. However, because it may be very difficult for clinicians to associate adverse patient outcomes with the use of defective Huber needles, there may be under-reporting of events.

The agency has issued a letter to manufacturers of other Huber needles to address design and manufacturing concerns.

“The agency’s laboratory work helped determine the coring problem, and we will continue to work with manufacturers to address coring issues as quickly and thoroughly as possible,” said Jeffrey Shuren, M.D., J.D., director of the FDA’s Center for Devices and Radiological Health.

The FDA continues to work closely with all 20 manufacturers of Huber needles to understand the potential causes for coring and identify corrective measures. While a more thorough investigation of this situation continues, the FDA recommends that health care professionals consider taking the following precautions, which will be posted on the FDA’s Web site, when accessing implanted ports with Huber needles:

Avoid flushing the syringe when initially confirming needles patency upon accessing the port. If the needle has cored the port, flushing may introduce the core into the patient’s body, and could lead to serious adverse events.
When possible, upon accessing the port, consider aspirating a small amount of blood from the port after septum puncture, then discard the syringe with its contents. This step may recapture the silicone sliver. If the needle becomes clogged when attempting to aspirate, remove the needle, discard it and select a new one.
Watch for signs and/or symptoms that may indicate damage to the port’s septum, such as medication leakage resulting in inadequate therapy delivery, along with tissue, nerve and/or muscle damage; and redness of the surrounding area.
Patients should continue to follow their doctor’s recommendations for receiving treatment.
Health care professionals and consumers may report serious adverse events (side effects) or product quality problems with the use of these products to the FDA’s MedWatch Adverse Event Reporting program either online, by regular mail, fax or phone.

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

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Posted By Jim Vititoe on February 3, 2010

Toyota Announces Comprehensive Plan to Fix Accelerator Pedals on Recalled Vehicles and Ensure Customer Safety

Toyota Motor Sales (TMS) U.S.A., Inc., announced it will begin fixing accelerator pedals in recalled Toyota Division vehicles this week.

Toyota’s engineers have developed and rigorously tested a solution that involves reinforcing the pedal assembly in a manner that eliminates the excess friction that has caused the pedals to stick in rare instances. Parts to reinforce the pedals are already being shipped for use by dealers, and dealer training is under way. Many Toyota dealers will work extended hours to complete the recall campaign as quickly and conveniently as possible, some even staying open 24 hours a day. The company has also taken the unprecedented action of stopping production of affected vehicles for the week of February 1.

Rigorously Tested Reinforced Pedals Will Eliminate the Excess Friction that Caused Sticking

Toyota Will Make Concerted Effort to Repair Recalled Vehicles as Quickly and Conveniently as Possible

TORRANCE, Calif., February 1, 2010 – Toyota Motor Sales (TMS) U.S.A., Inc., today announced it will begin fixing accelerator pedals in recalled Toyota Division vehicles this week. Toyota’s engineers have developed and rigorously tested a solution that involves reinforcing the pedal assembly in a manner that eliminates the excess friction that has caused the pedals to stick in rare instances. In addition, Toyota has developed an effective solution for vehicles in production.

Parts to reinforce the pedals are already being shipped for use by dealers, and dealer training is under way. Many Toyota dealers will work extended hours to complete the recall campaign as quickly and conveniently as possible, some even staying open 24 hours a day. The company has also taken the unprecedented action of stopping production of affected vehicles for the week of February 1.

“Nothing is more important to us than the safety and reliability of the vehicles our customers drive,” said Jim Lentz, president and Chief Operating Officer, TMS. “We deeply regret the concern that our recalls have caused for our customers and we are doing everything we can – as fast as we can – to make things right. Stopping production is never an easy decision, but we are 100% confident it was the right decision. We know what’s causing the sticking accelerator pedals, and we know what we have to do to fix it. We also know it is most important to fix this problem in the cars on the road.”

Lentz added: “We are focused on making this recall as simple and trouble-free as possible, and will work day and night with our dealers to fix recalled vehicles quickly. We want to demonstrate that our commitment to safety is as high as ever and that our commitment to our customers is unwavering.”

On January 21, Toyota announced its intention to recall approximately 2.3 million select Toyota Division vehicles equipped with a specific pedal assembly and suspended sales of the eight models involved in the recall on January 26.

Toyota vehicles affected by the recall include:
• Certain 2009-2010 RAV4
• Certain 2009-2010 Corolla
• 2009-2010 Matrix
• 2005-2010 Avalon
• Certain 2007-2010 Camry
• Certain 2010 Highlander
• 2007-2010 Tundra
• 2008-2010 Sequoia

No Lexus Division or Scion vehicles are affected by these actions. Also not affected are Toyota Prius, Tacoma, Sienna, Venza, Solara, Yaris, 4Runner, FJ Cruiser, Land Cruiser, Highlander hybrids and certain Camry models, including Camry hybrids, all of which remain for sale.

Further, Camry, RAV4, Corolla and Highlander vehicles with Vehicle Identification Numbers (VIN) that begin with “J” are not affected by the accelerator pedal recall.

In the event that a driver experiences an accelerator pedal that sticks in a partial open throttle position or returns slowly to idle position, the vehicle can be controlled with firm and steady application of the brakes. The brakes should not be pumped repeatedly because it could deplete vacuum assist, requiring stronger brake pedal pressure. The vehicle should be driven to the nearest safe location, the engine shut off and a Toyota dealer contacted for assistance.

Detailed information and answers to questions about issues related to this recall are available to customers at www.toyota.com/recall and at the Toyota Customer Experience Center at 1-800-331-4331.

How Toyota Will Fix Recalled Vehicles

Toyota has pinpointed the issue that could, on rare occasions, cause accelerator pedals in recalled vehicles to stick in a partially open position. The issue involves a friction device in the pedal designed to provide the proper “feel” by adding resistance and making the pedal steady and stable. The device includes a shoe that rubs against an adjoining surface during normal pedal operation. Due to the materials used, wear and environmental conditions, these surfaces may, over time, begin to stick and release instead of operating smoothly. In some cases, friction could increase to a point that the pedal is slow to return to the idle position or, in rare cases, the pedal sticks, leaving the throttle partially open.

Toyota’s solution for current owners is both effective and simple. A precision-cut steel reinforcement bar will be installed into the assembly that will reduce the surface tension between the friction shoe and the adjoining surface. With this reinforcement in place, the excess friction that can cause the pedal to stick is eliminated. The company has confirmed the effectiveness of the newly reinforced pedals through rigorous testing on pedal assemblies that had previously shown a tendency to stick.

Separately from the recall for sticking accelerator pedals, Toyota is in the process of recalling vehicles to address rare instances in which floor mats have trapped the accelerator pedal in certain Toyota and Lexus models (announced November 25, 2009), and is already notifying customers about how it will fix this issue. In the case of vehicles covered by both recalls, it is Toyota’s intention to remedy both at the same time.

####

MEDIA CONTACTS:
Toyota Motor Sales, Corporate Communications
(310) 468-5297
(310) 468-7359

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

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Posted By Jim Vititoe on February 3, 2010

FOR IMMEDIATE RELEASE
February 2, 2010
Release # 10-131 Firm’s Recall Hotline: (888) 810-1133
CPSC Recall Hotline: (800) 638-2772
CPSC Media Contact: (301) 504-7908
HC Media Contact: (613) 957-2983
Children’s Toy Jewelry Sets Recalled by Playmates Toys; Charms Violate the Total Lead Standard

WASHINGTON, DC – The U.S. Consumer Product Safety Commission and Health Canada, in cooperation with the firm named below, today announced a voluntary recall of the following products. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Tiny Tink and Friends Children’s Toy Jewelry Sets

Units: About 252,000

Importer: Playmates Toys, of Costa Mesa, Calif.

Hazard: A cylindrical metal connector on a charm can contain levels of total lead in excess of 300 ppm, which is prohibited under federal law.

Incidents/Injuries: None reported.

Description: This recall involves charms sold with the Tiny Tink and Friends toy jewelry sets. The charm is attached to a cord using a metal ring and cylinder and included with the sets as a separate accessory that children can attach to the toy necklace, bracelet or key chain. The toy jewelry sets containing the charm accessory were sold in a variety of styles:

Item # UPC # Description
74634 0 43377 74634 8 Tinker Bell’s Lil’ Tinker Bracelet
74641 0 43377 74641 6 Tinker Bell’s Lil’ Tinker Bracelet
74631 0 43377 74631 7 Rosetta’s Rosebud Key Chain
74632 0 43377 74632 4 Silvermist’s Water Lily Necklace
Charms that have plastic tabs instead of metal rings and cylinders are not included in this recall.

Sold at: Retailers nationwide from November 2008 through November 2009 for between $6 and $8.

Manufactured in: China

Remedy: Consumers should immediately take the charm and cord away from children, discard the items, and contact Playmates Toys for a replacement charm accessory.

Consumer Contact: For additional information, contact Playmates toys at (888) 810-1133 between 9 a.m. and 5 p.m. PT Monday through Friday or visit the firm’s Web site at www.playmatestoys.com

Note: Health Canada’s press release is available at http://cpsr-rspc.hc-sc.gc.ca/PR-RP/recall-retrait-eng.jsp?re_id=954

Note: CPSC was alerted to this hazard by the State Attorney General of California

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

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Posted By Jim Vititoe on February 3, 2010

FOR IMMEDIATE RELEASE
February 2, 2010
Release # 10-130 Firm’s Recall Hotline: (800) 437-9560
CPSC Recall Hotline: (800) 638-2772
CPSC Media Contact: (301) 504-7908
Children’s Jackets with Drawstrings Recalled by GTM Sportswear Due to Strangulation Hazard

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Children’s Jackets with Drawstrings

Units: About 210,000

Manufacturer/Importer: GTM Sportswear Inc., of Manhattan, Kan.

Hazard: The children’s jackets have drawstrings through the hood which can pose a strangulation hazard to children. In February 1996, CPSC issued guidelines (pdf) (which were incorporated into an industry voluntary standard in 1997) to help prevent children from strangling or getting entangled on the neck and waist drawstrings in upper garments, such as jackets or sweatshirts.

Incidents/Injuries: None reported.

Description: This recall involves children’s hooded nylon jackets in sizes XXS-XL (2T-16) and in various colors. “GTM Sportswear” is printed on a label sewn in the neck of the garments. Styles include Youth Medalist Jacket (YJA180), Youth Legacy Jacket (YJAPT01), Youth Eclipse Jacket (YLJA186), Youth Dominator Jacket (YJA3800), Youth Booster Jacket (YJA150), Youth Achiever Jacket (YJA161).

Sold at: GTM Sportswear, K-State Super Store, and Cats Closet stores in Kansas, other customer screen print and embroidery stores nationwide, on the Web at www.gtmsportswear.com, www.kstategear.com, www.catscloset.com and www.justforkix.com and in GTM Sportswear and the Just for Kix catalogs from January 2003 through December 2009 for between $25 and $30.

Manufactured in: China

Remedy: Consumers should immediately remove the drawstrings from the jackets to eliminate the hazard or return the jackets to their place of purchase or to GTM Sportswear for a full refund.

Consumer Contact: For additional information, contact GTM Sportswear at (800) 437-9560 between 7 a.m. and 7 p.m. CT Monday through Friday, and on Saturday between 8 a.m. and 1 p.m., or visit the firm’s Web site at www.gtmsportswear.com

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

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Posted By Jim Vititoe on February 3, 2010

FOR IMMEDIATE RELEASE
February 2, 2010
Release # 10-129 Firm’s Recall Hotline: (888) 899-0888
CPSC Recall Hotline: (800) 638-2772
CPSC Media Contact: (301) 504-7908
Children’s Hooded Sweatshirts with Drawstrings Recalled by New Mode Sportswear Due to Strangulation Hazard

WASHINGTON, D.C. - The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: 21 Pro USA Children’s Pullovers and Hoodies

Units: About 7,200

Distributor: New Mode Sportswear, of Garden Grove, Calif.

Hazard: The children’s sweatshirts have a drawstring through the hood which can pose a strangulation hazard to children. In February 1996, CPSC issued guidelines (pdf) (which were incorporated into an industry voluntary standard in 1997) to help prevent children from strangling or getting entangled on the neck and waist drawstrings in upper garments, such as jackets or sweatshirts.

Incidents/Injuries: None reported.

Description: This recall involves children’s hooded pullover and zip hooded sweatshirts in sizes S-XL. They were sold in black, navy blue and heather gray. Brand name “21 Pro USA” Sportswear and RN#92952 are printed on a label sewn into the neck of the sweatshirts.

Sold at: Various T-shirt outlets and swap meets on the West Coast from January 2006 through July 2006 for about $6.

Manufactured in: China

Remedy: Consumers should immediately remove the drawstrings from the sweatshirts to eliminate the hazard or return the garments to the place of purchase or to New Mode Sportswear for a full refund.

Consumer Contact: For additional information, contact New Mode Sportswear toll-free at (888) 899-0888 between 8 a.m. and 4:30 p.m. PT Monday through Friday, or visit the firm’s Web site at www.21prousa.com

If you have been seriously injured by the above event, please visit the products liability lawyers at Masry & Vititoe for a case evaluation. Through experience and education, Masry and Vititoe is able to expertly evaluate medical injuries and pursue personal injury claims on behalf of the injured plaintiff.

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