XYMOGEN® of Orlando, FL is recalling specific lots of 3 Varieties of OrganiX Bars: Omega-3, Spice and Greens, because they may contain undeclared peanut protein. People who have an allergy or severe sensitivity to peanut protein run the risk of serious or life-threatening allergic reaction if they consume these products.
Merrick Pet Care Recalls Doggie Wishbone (Item #29050, Lot 11031 Best by 30 Jan 2013) Because of Possible Salmonella Health Risk
Merrick Pet Care, Inc. of Amarillo, Texas is recalling a single lot of its Doggie Wishbone pet treat (ITEM # 29050, UPC # 2280829050, Lot 11031 Best By 30 Jan 2013) because they have the potential to be contaminated with Salmonella. Merrick Pet Care has made the decision to recall the Doggie Wishbone pet treats in the abundance of caution.
Fresh & Easy Neighborhood Market Voluntarily Recalls One Date Code Of f&eâ„¢ Brand Organic Baby Spinach Because Of Possible Health Risk
Fresh & Easy Neighborhood Market Inc., is voluntarily recalling fresh Organic Baby Spinach with the Enjoy by date of Aug 01 sold under the f&eâ„¢ label.
The recall notification is being issued out of an abundance of caution based on a random sample test, conducted on behalf of the Food & Drug Administration (FDA).
Winn-Dixie Issues Voluntary Recall On Specific In-Store Bakery Items Due To Mislabeling And Undeclared Allergens
Winn-Dixie Stores, Inc., is voluntarily recalling from its in-store bakeries the following items because the products may be mislabeled:The mislabeled products may contain undeclared egg and/or wheat.
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Transpecos Foods, LP Issues Allergy Alert on Undeclared Soy Allergen in Cheddar Cheese Jalapeno Bites and Cream Cheese Jalapeno Bites
Transpecos Foods, LP of Pecos, Texas is recalling the following items because they may contain undeclared Soy allergens: People who have an allergy or sensitivity to Soy allergens run the risk of an allergic reaction if they consume these products.
FDA approves the first specific treatment for scorpion stings
The U.S. Food and Drug Administration today approved Anascorp, the first specific treatment for a scorpion sting by Centruroides scorpions in the United States.
American Regent, Inc. Initiates Voluntary Recall of Seventeen Lots of Vasopressin Injection, USP, Multiple Dose Vials due to Sub-Potency
American Regent, Inc. is conducting a nationwide voluntary recall of 5 lots of Vasopressin Injection, USP 20 units/mL (200 units/10mL), 10 mL Multiple Dose Vials; 11 lots of Vasopressin Injection, USP 20 units/mL, 1 mL Multiple Dose Vials; and 1 lot of Vasopressin Injection, USP 10 units/0.5 mL,0.5 mL Multiple Dose Vials to the Retail/Hospital level.
FDA, international counterparts report progress on drug inspection collaboration
FDA, international counterparts report progress on drug inspection collaboration
FDA reopens comment period on proposed ‘gluten-free’ food labeling rule
The U.S. Food and Drug Administration today reopened the comment period for its 2007 proposal on labeling foods as “gluten-free.” The agency is also making available a safety assessment of exposure to gluten for people with celiac disease (CD) and invites comment on these additional data.
Voluntary Worldwide Field Corrective Action of the Vital Signs Hygroscopic Condenser Humidifier (HCH) / Anesthesia Breathing Circuit
In April 2011, Vital Signs Devices, a GE Healthcare Company, initiated a voluntary worldwide field correction of the Vital Signs Hygroscopic Condenser Humidifier (HCH)/Anesthesia Breathing Circuit. This device is sold under various part numbers – see list below.