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. It is illegal to resell or attempt to resell a recalled consumer product. Name of … [Read more...]
Fleetwood RV, Inc. Equipment:other:labels Recall
Vehicle Make / Model:FLEETWOOD / BOUNDER CLASSIC Model Year(s):2012-2013 Manufacturer: Fleetwood RV, Inc.Report Receipt Date: JAN 09, 2013NHTSA CAMPAIGN ID Number: 13V007000NHTSA Action Number: N/AComponent: EQUIPMENT:OTHER:LABELSPotential Number of Units Affected: 14Summary:Fleetwood RV is recalling certain model year 2012 and 2013 … [Read more...]
Target Recalls Hand-Held Air Misters Due to Injury 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. It is illegal to resell or attempt to resell a recalled consumer product. Name of … [Read more...]
Goshen Coach Equipment Recall
Vehicle Make / Model:GOSHEN / G-FORCEGOSHEN / GC IIGOSHEN / GC II-550GOSHEN / PACERGOSHEN / PACER LSGOSHEN / PACER LTDGOSHEN / SENTINEL Model Year(s):2011-20122006-20122007-20092006-20122008 2010 201320122011 Manufacturer: Goshen CoachReport Receipt Date: JAN 14, 2013NHTSA CAMPAIGN ID Number: 13V008000NHTSA Action Number: N/AComponent: … [Read more...]
Eldorado National- Kansas Equipment Recall
Vehicle Make / Model:ELDORADO / AEROTECH 240 Model Year(s):2012 Manufacturer: Eldorado National- KansasReport Receipt Date: JAN 14, 2013NHTSA CAMPAIGN ID Number: 13V009000NHTSA Action Number: N/AComponent: EQUIPMENTPotential Number of Units Affected: 21Summary:Eldorado National is recalling certain model year 2012 Aerotech 240 buses … [Read more...]
FDA Warns Durata Quality Control Problems Could Lead to Fines or Worse for St. Jude
Last week, the FDA warned manufacturer St. Jude that quality control and design problems related to the Durata ICD lead must be resolved within 15 days from the date of the letter (January 10) or the firm would face additional action, such as fines, seizures, or injunctions against selling the leads or other products. In a report to the Securities … [Read more...]
Alabama Court Rules Man Taking Generic Drug Can Sue Name Brand Manufacturer
Since the US Supreme Court decision in Pliva v. Mensing barred most lawsuits against generic drug manufacturers, it seemed that people injured by generic drugs that lacked adequate labeling may have no right to compensation. On Friday January 11, though, the Alabama Supreme Court proposed a logical solution to the problem: people injured by generic … [Read more...]
Advance Pharmaceutical Rcalls One Lot (# 12G468) of Ferrous Sulfate Tablets, 325 mg, that may actually contain Meclizine HCl 25 mg tablets
Advance Pharmaceutical Inc. today announced that it is conducting a voluntary nationwide recall of one lot of Ferrous Sulfate Tablets, 325 mg, Lot 12G468 Exp. 07/14, UPC Barcode 0 0536-5890-01 3. The lot was manufactured and packaged in 100 count bottles by Advance Pharmaceutical Inc. under the label of Rugby NATURAL IRON SUPPLEMENT Ferrous … [Read more...]
Belmont Confections Issues Allergy Alert on Undeclared Peanuts in “Dymatize Nutrition, Elite Gourmet Bars” (Cookies & Cream and Fudge Brownie)
Belmont Confections Inc. is recalling Dymatize Nutrition Elite Gourmet Cookies & Cream bars and Dymatize Nutrition Elite Gourmet Fudge Brownie bars in both the 1.5oz and 3oz packages because they may contain undeclared peanuts. Belmont became aware of the problem via a complaint to the distributor Dymatize Inc. People who have allergies to … [Read more...]
Homestead Creamery Artisan Cheese Removed from Store Shelves
The State Milk Board, in conjunction with the Missouri Department of Agriculture and the Missouri Department of Health and Senior Services, announced today that Homestead Creamery of Jamesport, Mo. is voluntarily withdrawing a batch of its Flory's Favorite cheese from the marketplace. Preliminary test results received from the Missouri State Health … [Read more...]
Milo’s Kitchen® Voluntarily Recalls Chicken Jerky and Chicken Grillers Home-style Dog Treats
Milo's Kitchen® today announced that it is voluntarily recalling its Chicken Jerky and Chicken Grillers home-style dog treats from retailer shelves nationally. No other Milo's Kitchen® products are affected. On Monday, New York State's Department of Agriculture informed the U.S. Food and Drug Administration (FDA) and the Company that trace amounts … [Read more...]
Boba Direct Issues Allergy Alert on Undeclared Milk in BD Flavored Powders
Boba Direct (BD) announced the voluntary recall of the following BD Flavored Powders: Almond, Avocado, Banana, Blueberry, Cafe Latte, Cherry, Chocolate, Coconut, Honeydew, Lavender, Lychee, Mango, Matcha Green Tea, Milk Tea, Passionfruit, Peppermint, Pineapple, Red Bean, Strawberry, Taro, Vanilla and Watermelon in the 2.2 lb. plastic bags because … [Read more...]
Island Delights Voluntarily Recalls Island Delights Coconut Haystack Candy Due to Undeclared Milk
Contact Consumer Gregory Miller or Ann Crall 1-866-887-4100 FOR IMMEDIATE RELEASE - Seville, OH - January 9, 2013 - Island Delights, Inc. today recalled 492 Bags of its Coconut Haystack Candy due to mislabeling and undeclared allergens. This was discovered during an audit from the Ohio Department of Agriculture on January 7, 2013. The Coconut … [Read more...]
Product Recall Because of Possible Listeria Monocytogenes Risk
As precautionary measure, Delifish has decided to expand the voluntary recall to include cold smoked products related to Julian dates 235 to 345, the previous voluntary recall included cold smoked products related to Julian dates 249- 291. There have been no new detections on products placed on the market in relation to this expansion. The … [Read more...]
FDA Warns LASIK Providers about Lack of Risk Information
On December 18, the FDA sent warning letters to five LASIK providers that they are failing to provide adequate information about risks to potential patients. This targeted follow-up comes after more than three years of communication with eye care professionals about failing to give consumers adequate information to make informed decisions about … [Read more...]
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