Kimberly-Clark Recalls Kotex Natural Balance* Security® Unscented Tampons Regular Absorbency from a Limited Number of Retail Stores Within the United States
November 10, 2011 by Allen Sanford
Filed under FDA Recalls
Short Summary: Kimberly-Clark announced a product recall of a limited number of its Kotex Natural Balance* Security® Unscented Tampons Regular Absorbency distributed to specific stores in the United States. This recall is limited to two product SKUs (carton codes), 15063 (18 count) and 15068 (36 count). Read the FDA’s full release by clicking here. Baby [...]
Rite Aid Voluntarily Recalls 12 oz. Tins of Rich Fields Butter Cookies
October 29, 2011 by Allen Sanford
Filed under FDA Recalls
Short Summary: Working in consultation with the United States Food and Drug Administration, Rite Aid has initiated a voluntary chainwide recall of approximately 85,000 tins of butter cookies distributed by Rite Aid under the Rich Fields brand name because of the possibility of contamination with Bacillus cereus. Read the FDA’s full release by clicking here. [...]
CooperVision Continues the Voluntary Recall of Avaira™ Toric Contact Lenses
October 14, 2011 by Allen Sanford
Filed under FDA Recalls
Short Summary: In full cooperation with the United States Food and Drug Administration, CooperVision, Inc. is continuing to work with the FDA, distributors, customers, eye care practitioners and lens wearers to complete the worldwide recall initiated on August 19, 2011 on certain lots of Avaira™ Toric contact lenses. Read the FDA’s full release by clicking [...]
Andrew Williamson Fresh Produce Announces Precautionary Recall of Organic Grape Tomatoes Due to Possible Health Risk
September 28, 2011 by Allen Sanford
Filed under FDA Recalls
Short Summary: Andrew Williamson Fresh Produce is voluntarily recalling one lot of organic grape tomatoes sold under the Limited Edition® and Fresh & Easy labels due to a possible health risk from Salmonella. The recall notice is being issued out of an abundance of caution because one clamshell of Limited Edition organic grape tomatoes tested [...]
Unilever United States, Inc. Issues Allergy Alert for Mislabeled 24-Count Boxes of Popsicle® Sugar Free Orange, Cherry and Grape Flavor Due to Undeclared Milk
August 12, 2011 by Allen Sanford
Filed under FDA Recalls
Short Summary: Unilever United States, Inc. is voluntarily recalling a limited number of mislabeled 24-count boxes of Popsicle® brand Sugar Free Orange, Cherry and Grape flavored ice pops that mistakenly contain Popsicle® brand Sugar Free Healthy Bunch® Fudgsicle® and Creamsicle® ice pops. Read the FDA’s full release by clicking here. Baby Life Magazine posts press [...]
Unilever United States, Inc. Issues Allergy Alert for Mislabeled 24-Count Boxes of Popsicle® Sugar Free Orange, Cherry and Grape Flavor Due to Undeclared Milk
August 11, 2011 by Allen Sanford
Filed under FDA Recalls
Short Summary: Unilever United States, Inc. is voluntarily recalling a limited number of mislabeled 24-count boxes of Popsicle® brand Sugar Free Orange, Cherry and Grape flavored ice pops that mistakenly contain Popsicle® brand Sugar Free Healthy Bunch® Fudgsicle® and Creamsicle® ice pops. Read the FDA’s full release by clicking here. Baby Life Magazine posts press [...]
Defibtech Announces a Voluntary Recall of DDU-100 series AEDs
May 2, 2011 by Allen Sanford
Filed under FDA Recalls
Short Summary: Defibtech, LLC is initiating a worldwide voluntary recall of certain DDU-100 series semi-automatic external defibrillators (AEDs) sold under the Lifeline AED and ReviveR AED brand names, including 65,885 AEDs distributed in the United States. This recall affects only DDU-100 Series AEDs shipped with 2.004 software or earlier. Read the FDA’s full release by [...]
Lilly Announces Important Action Regarding Recall of Alcohol Prep Pads Made by Triad Group Included in Forteo Starter Kits
March 18, 2011 by Allen Sanford
Filed under FDA Recalls
Short Summary: Eli Lilly and Company (NYSE: LLY) announced today that patients should not use the alcohol prep pads made by the Triad Group that are contained in the black starter kits for Forteo® [teriparatide (rDNA origin) injection] in the United States. The Tri-ad Group is recalling the alcohol prep pads due to potential contamination [...]
Neuro Resource Group, Inc. Informs Customers of Important Information about Triad Group’s Alcohol Prep Pads
February 10, 2011 by Allen Sanford
Filed under FDA Recalls
Short Summary: Neuro Resource Group, Inc. (NRG) has become aware of the market recall of Triad Group’s alcohol prep pads, alcohol swabs, and alcohol swabsticks manufactured by Triad in the United States and marketed under various brand names. The Triad Group alcohol prep pads are co-packaged and distributed with NRG devices to customers in the [...]
Important Information for Extavia® (interferon beta 1-b) Patients Regarding Triad Group’s Alcohol Prep Products
January 31, 2011 by Allen Sanford
Filed under FDA Recalls
Short Summary: Novartis Pharmaceuticals Corporation (Novartis) has become aware of a United States market recall of all lots of alcohol prep pads, swabs and swabsticks manufactured by the Triad Group and marketed under various brand names. The recall has been initiated due to concerns about potential microbial contamination of the alcohol products with Bacillus cereus, [...]