Frontier Natural Products Co-op Initiates Voluntary Recall Due to Possible Health Risk from Nutmeg
In response to a recall commenced by its supplier (Mincing Overseas Spice Company, Dayton, New Jersey), Frontier Natural Products Co-op, is voluntarily recalling two products manufactured with non-organic nutmeg that were sold under the Frontier brand and under the Whole Foods Market brand listed below that contain nutmeg supplied by Mincing Overseas Spice Company. The nutmeg has the potential to be contaminated with Salmonella.
B. Braun addEASE Binary Connector: Class I Recall -Stopper Fragments May Enter Bag
The particles in the solution can potentially enter a patient’s body and lead to serious adverse health consequences.
Senate Passes Overhaul of Food Safety Regulations
Senate Passes Overhaul of Food Safety Regulations - NYTimes.com
WASHINGTON — The Senate on Tuesday passed a sweeping overhaul of the nation’s food-safety system, after recalls of tainted eggs, peanut butter and spinach that sickened thousands and led major food makers to join consumer advocates in demanding stronger government oversight.
McCormick & Company Recalls Golden Dipt® Fry Easy All-Purpose Batter Due To Unlabeled Egg Ingredient
McCormick & Company, Incorporated (NYSE:MKC) has announced a voluntary recall of Golden Dipt® Fry Easy All-Purpose Batter, 10 OZ, with UPC Code 4123470111 and “BEST BY” date of NOV 17 11 AH. A very limited number of packages of Golden Dipt® All-Purpose Batter with this date code contain an undeclared egg ingredient.
HiRes 90K Cochlear Implant Device: Recall - Malfunction
Two confirmed instances where the product experienced a malfunction, recipients experienced severe pain, overly loud sounds and/or shocking sensations.
Recall of Tylenol Cold Liquid Products
In consultation with the U.S. Food and Drug Administration (FDA), McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc., is recalling, from the wholesale and retail level, three TYLENOL® Cold Multi-Symptom liquid products in order to update the labeling for these products. The specific products involved, listed below, are sold in the United States.
Recall of Children’s BENADRYL® Allergy FASTMELT® Tablets and Junior Strength MOTRIN® Caplets
In consultation with the U.S. Food and Drug Administration (FDA), McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc. has initiated a voluntary recall of all product lots of Children’s BENADRYL® Allergy FASTMELT® Tablets, in cherry and grape flavors, that were distributed in the United States, Belize, Barbados, Canada, Puerto Rico, St. Martin, and St. Thomas and all product lots of Junior Strength MOTRIN® Caplets, 24 count, that were distributed in the United States.
Recall of ROLAIDS® Extra Strength Softchews
In consultation with the U.S. Food and Drug Administration (FDA), McNeil Consumer Healthcare, Division of McNEIL-PPC, Inc. has initiated a voluntary recall of one product lot of ROLAIDS® Extra Strength Softchews, Cherry Flavor, 36 count package distributed in the United States.
MONACO COACH ( 10V588000 )
Dated: NOV 17, 2010 NAVISTAR IS RECALLING CERTAIN RECREATIONAL VEHICLES EQUIPPED WITH 1200-SERIES NORCOLD REFRIGERATORS. THE POPULATION OF REFRIGERATORS BEING ADDRESSED CONTAINS EITHER A SENSING ALGORITHM OR THERMAL SWI…
SAFARI COACH ( 10V588000 )
Dated: NOV 17, 2010 NAVISTAR IS RECALLING CERTAIN RECREATIONAL VEHICLES EQUIPPED WITH 1200-SERIES NORCOLD REFRIGERATORS. THE POPULATION OF REFRIGERATORS BEING ADDRESSED CONTAINS EITHER A SENSING ALGORITHM OR THERMAL SWI…