Search Results for: labeling

Nassau Candy Issues Nationwide Allergy Alert Because Of Possible Undeclared Allergens on their Tasty Dish Snack Tubs of Chocolate Almonds, Chocolate Raisins and Sour Neon Worms

November 20, 2009 By The FDA Leave a Comment

Nassau Candy Distributors of Hicksville, New York, is voluntarily recalling possibly unlabeled pegable snack tubs because they contain the following undeclared allergens; Tree Nuts {Almonds}, Soy and Milk and may contain the following undeclared allergens Peanuts, other Tree Nuts {brazil nuts, walnuts, filberts, hazelnuts, pecans, pistachios, … [Read more...]

SNACKS ON RACKS Issues Nationwide Allergy Alert because of Undeclared Allergens in Their Gourmet Snacks Pack Product Line

November 18, 2009 By The FDA Leave a Comment

RECALLS, MARKET WITHDRAWALS, & SAFETY ALERTS ARCHIVE FOR RECALLS, MARKET WITHDRAWALS & SAFETY ALERTS ENFORCEMENT REPORTS INDUSTRY GUIDANCE MAJOR PRODUCT RECALLS - RECALL -- FIRM PRESS RELEASE FDA POSTS PRESS RELEASES AND OTHER NOTICES OF RECALLS AND MARKET WITHDRAWALS FROM THE FIRMS INVOLVED AS A SERVICE TO CONSUMERS, THE MEDIA, AND OTHER … [Read more...]

BYETTA Kidney Failure Risk

November 5, 2009 By E. Sizemore 3 Comments

The FDA has announced labeling changes on the diabetes drug BYETTA (exenatide). The revisions will warn doctors and patients of the risk of kidney failure and renal insufficiency when taking the medication. So far there have been at least four reported deaths from kidney failure associated with BYETTA use. This is not the first significant health … [Read more...]

TRANS TECH ( 09V416000 )

November 1, 2009 By US Recall News Leave a Comment

Vehicle Make / Model: Model Year(s): TRANS TECH / MFSAB 2007-2009 Manufacturer: TRANS TECH BUS Mfr's Report Date: OCT 22, 2009 NHTSA CAMPAIGN ID Number: 09V416000 N/A NHTSA Action Number: N/A Component: EQUIPMENT:OTHER:LABELS Potential Number of Units … [Read more...]

FDA Alert: New USP Standards for Heparin Products Will Result in Decreased Potency

October 2, 2009 By The FDA 1 Comment

The U.S. Food and Drug Administration (FDA) is alerting healthcare providers of a change to the United States Pharmacopeia (USP) monograph for heparin, effective October 1, 2009. Manufacturers will not begin shipping heparin products manufactured and tested according to the new USP monograph until October 8th or later. This change—largely in … [Read more...]