Vehicle Make / Model: Model Year(s): MACK / CX 1999-2005 MACK / CXN 2004-2008 Manufacturer: MACK TRUCKS, INC Mfr's Report Date: DEC 23, 2008 NHTSA CAMPAIGN ID Number: 08V688000 N/A NHTSA Action Number: N/A … [Read more...]
Missouri Firm Recalls Sausage Products For Possible Listeria Contamination
Recall Release CLASS I RECALL FSIS-RC-052-2008 HEALTH RISK: HIGH Congressional and Public Affairs (202) 720-9113 Peggy Riek WASHINGTON, Dec. 25, 2008 - T. Piekutowski European Style Sausage, a St. Louis, Mo., firm, is recalling approximately 750 pounds of sausage products that may be contaminated with Listeria monocytogenes, the U.S. … [Read more...]
KRC Food Trading Inc. Recall of Fish Cake Sushi
CONTACT: MS JOANNA KIM 1-213-388-8215 FOR IMMEDIATE RELEASE DECEMBER 23, 2008--LOS ANGELES, CA--KRC FOOD TRADING INC IS RECALLING ITS FISH CAKE SUSHI WITH PRODUCTION DATE OF DECEMBER 19 AND DECEMBER 22 DUE TO THE LABEL NOT DECLARING EGGS. PEOPLE WHO HAVE AN ALLERGY OR SEVERE SENSITIVITY TO EGGS RUN THE RISK OF SERIOUS OR LIFE-THREATENINGALLERGIC … [Read more...]
ETHEX Recalls One Lot of Hydromorphone HCl 2 mg Tablets
Note: This is in addition to the previous ETHEX recall from last month for the pharmaceutical drugs: Propafenone, Isosorbide, Morphine and Destroamphetamine due to the possibility of oversized pills. CONTACT: ANN MCBRIDE 1-800-748-1472 FOR IMMEDIATE RELEASE -- ST. LOUIS, MO – DECEMBER 23, 2008 – ETHEX CORPORATION ANNOUNCED TODAY THAT IT HAS … [Read more...]
KV Pharmaceutical Suspends Shipments on All Drugs in Pill Form Including Hydromorphone
Note: Also see related ETHEX Hydromorphone Recall CONTACT: CATHERINE BIFFIGNANI (314) 645-6600 FOR IMMEDIATE RELEASE --ST. LOUIS – DEC. 23, 2008 – KV PHARMACEUTICAL HAS ADVISED THE U.S. FOOD AND DRUG ADMINISTRATION (FDA) THAT, EFFECTIVE MIDNIGHT DEC. 19, 2008, THE COMPANY VOLUNTARILY SUSPENDED ALL SHIPMENTS OF ALL FDA APPROVED DRUG PRODUCTS IN … [Read more...]
Foursquare Recalls Hooded Youth Jackets with Drawstrings 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: FOURSQUARE HOODED JACKETS UNITS: ABOUT 1,300 DISTRIBUTORS: FOURSQUARE … [Read more...]
Hallmark Recalls Jumbo Snow Globes Due to Fire 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: JUMBO SNOWMAN SNOW GLOBES UNITS: 7,000 IMPORTER: HALLMARK CARDS INC., … [Read more...]
Gardener's Supply Company Recalls Candle-Powered Carousels Due to Fire 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: CANDLE-POWERED CAROUSELS UNITS: ABOUT 1,500 IMPORTER: GARDENER’S … [Read more...]
Munire Recalls Newport Cribs Due to Violation of Lead Paint Standards
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: NEWPORT RUBBED BLACK 4-IN-1 CRIBS AND MATCHING FURNITURE UNITS: ABOUT … [Read more...]
Woodstock Percussion Recalls Toy Drums for Lead Paint
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: CALYPSO STEEL DRUMS UNITS: ABOUT 2,800 MANUFACTURER: WOODSTOCK … [Read more...]
Magura USA Recalls Bicycle Suspension Forks Due to Crash Hazard
THE FOLLOWING PRODUCT SAFETY RECALL WAS VOLUNTARILY CONDUCTED BY THE FIRM IN COOPERATION WITH THE CPSC. CONSUMERS SHOULD STOP USING THE PRODUCT IMMEDIATELY UNLESS OTHERWISE INSTRUCTED. NAME OF PRODUCT: DURIN RACE 80/100 BICYCLE SUSPENSION FORKS UNITS: ABOUT 320 IMPORTER: MAGURA USA, OF OLNEY, ILL. MANUFACTURER: GUSTAV MAGENWIRTH GMBH & CO. KH, OF … [Read more...]
Teknion Recalls to Repair Office Chairs Due to Fall Hazard
THE FOLLOWING PRODUCT SAFETY RECALL WAS VOLUNTARILY CONDUCTED BY THE FIRM IN COOPERATION WITH THE CPSC. CONSUMERS SHOULD STOP USING THE PRODUCT IMMEDIATELY UNLESS OTHERWISE INSTRUCTED. NAME OF PRODUCT: CONTESSA OFFICE CHAIRS (SEE PHOTO “A”) UNITS: ABOUT 60,000 DISTRIBUTOR: TEKNION LLC, OF TORONTO, CANADA MANUFACTURER: OKAMURA CORP., OF JAPAN … [Read more...]
Atomic Skis USA Recalls Ski Bindings Due to Unexpected Release
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: ALPINE SKI BINDINGS UNITS: ABOUT 125,000 (AN ADDITIONAL 1.0 MILLION … [Read more...]
Dangerous Weight Loss Products and Diet Pills Being Sold Online
The FDA says it may pursue criminal action against several companies that produce over-the-counter (OTC) weight loss supplements because these companies are refusing to take their dangerous diet pills off the shelves. In the meantime, FDA is urging consumers not to use any of the weight loss and diet products below, as they may contain undeclared, … [Read more...]
Calls for Recall of Bard Avaulta and Other Surgical Mesh Products Continue
Many women thought their health issues were unique until the FDA issued a warning about transvaginal surgical mesh products in late October, citing over one-thousand reports of complications relating to nine different surgical mesh manufacturers, including Bard Avaulta. Note: The FDA has issued another surgical mesh warning in July 2011. Side … [Read more...]
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