7-Eleven, Inc. of Irving, TX is recalling fully baked chocolate chunk, sugar and oatmeal raisin cookies produced by CSM Bakery Solutions frozen cookie pucks because they may contain undeclared peanut. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Category Archives: Food & Drug Recalls
Bakery Express of Central FL., Inc. Issues Alleregy Alert on Undeclared Peanuts in 7-Eleven Fresh to Go Cookies
Bakery Express of Central FL., Inc of Orlando, Florida is recalling select 7-ELEVEN FRESH TO GO cookies, because they may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
FDA approves first generic Crestor
The U.S. Food and Drug Administration today approved the first generic version of Crestor (rosuvastatin calcium) tablets for the following uses
World’s Choice Products, Inc. Issues Allergy Alert on Undeclared Milk And Soy Lecithin From Whey Protein in “Supreme Elixir”, “Kids Juice” And “Xtreme Fiber Detox”
World’s Choice Products, Inc. of San Diego, CA, is recalling the following products: 32 fluid ounce Supreme Elixir drink, 32 fluid ounce Kid’s Juice, 1 pound and 8 ounce Xtreme Fiber Detox. The recall was initiated because the products contain undeclared whey protein, which contains the allergens of milk and soy lecithin.
Southeastern Grocers Issues Voluntary Recall on Undeclared Peanuts in Bakery Creme Cakes
Southeastern Grocers, the parent company of BI-LO, Harveys and Winn-Dixie stores, is voluntarily recalling its 32 ounce Bakery Creme Cakes and 14 ounce Bakery Sliced Creme Cakes, because the products may contain undeclared peanuts.
Old Home Kitchens Issues Allergy Alert and Voluntary Recall on Undeclared Peanuts in "Old Home Kitchens 14oz Sliced Creme Cake"
Old Home Kitchens is voluntarily recalling “Old Home Kitchens 14oz. Sliced Lemon Creme Cake production code 16104” “Old Home Kitchens 14oz. Sliced Vanilla Creme Cake production code 16104,” and “Old Home Kitchens 14oz. Sliced Strawberry Swirl Creme Cake with a production code of 16098” ink jet coded on plastic clam shell package, due to a potential presence of peanut allergen in a CSM Bakery Solutions supplied ingredient. People who have allergy or sensitivity to peanuts run the risk of serious or life threatening allergic reaction if they consume these products.
Bakery Express of Southern California Issues Allergy Alert on Undeclared Peanut in 7-Eleven Fresh To Go Cookies
Bakery Express of Southern California of Fullerton, CA is recalling 7-ELEVEN FRESH TO GO brand cookies, because it may contain undeclared peanuts. People who have an allergy or severe sensitivity to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products.
Schaffner Distributing Pronutri LLC. Issues an Allergy Alert on Undeclared Soy Lecithin and Milk in Re-VITA-lize
Schaffner Distributing Pronutri LLC. is recalling Re-VITA-lize LOT #15554, because it contains undeclared SOY Lecithin and MILK ingredient. People who have an allergy or severe sensitivity to SOY OR MILK ingredients may run the risk of serious or life-threatening allergic reaction if they consume these products.
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Glenn Wayne Wholesale Bakery Issues Allergy Alert on Undeclared Peanuts in Select 7-Eleven Fresh To Go Cookies
Glenn Wayne Wholesale Bakery of Bohemia, NY, is recalling select 7-ELEVEN FRESH TO GO brand cookies because they may contain undeclared peanuts. People who have an allergy to peanuts run the risk of serious or life-threatening allergic reaction if they consume these products
Fresenius Kabi Issues Voluntary Nationwide Recall of Sensorcaine® -MPF (bupivacaine HCl) Injection, USP due to the Presence of Particulate Matter Characterized as Glass
Fresenius Kabi USA announced today it is voluntarily recalling a single lot (Lot Number 6111504; Product Code 470237) of Sensorcaine-MPF (bupivacaine HCl) Injection, USP, 0.75%, 7.5 mg/mL, 30 mL fill in a 30 mL vial. The recall is being performed to the user level due to visible particulate matter characterized as glass observed by the company during inspection of reserve samples.