Silver Spring, Maryland—(ENEWSPF)—October 5, 2017 Authored by: U.S. Food & Drug Administration (FDA) Sid Wainer & Son® of New Bedford, MA is voluntarily recalling Jansal Valley® brand Dried Chili De Arbol Peppers because it does not have the proper allergens identified, being peanuts. People who have an allergy or severe sensitivity to peanuts run[Read More…]
Recalls
Silver Spring Foods, Inc. Voluntarily Recalls Waterfront Bistro Tartar Sauce
Silver Spring, Maryland—(ENEWSPF)—September 28, 2017 Authored By: Food & Drug Administration (FDA) Silver Spring Foods, Inc. is voluntarily recalling Waterfront Bistro Tartar Sauce because there is a chance an incorrect back label was attached to the bottle, which does not correctly identify ingredients that could pose an allergen risk; specifically,[Read More…]
Recall of Certain Lexus and Toyota Land Cruisers
Washington, DC—(ENEWSPF)—September 26, 2017 Summary Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2008-2016 Toyota Land Cruiser, 2006 Lexus LX470, and 2008-2013 Lexus LX570 vehicles. These vehicles may be equipped with an incorrect driver or front passenger air bag. As such, these vehicles fail to comply with the requirements[Read More…]
Ford Motor Company Recalls Certain 2017 F-150 and Mustang Vehicles
Washington, DC—(ENEWSPF)—September 15, 2017 Summary Ford Motor Company (Ford) is recalling certain 2017 F-150 and Mustang vehicles. The air bag inflator within the passenger frontal air bag module may rupture in the event of a crash. Remedy Ford will notify owners, and dealers will replace the passenger frontal air bag[Read More…]
Target Recalls Room Essentials 4-Drawer Dressers Due to Tip-Over and Entrapment Hazards
Washington, DC–(ENEWSPF)–September 14, 2017 Recall Summary Name of product: Room Essentials 4-drawer dressers Hazard: The recalled dressers are unstable if they are not anchored to the wall, posing serious tip-over and entrapment hazards that can result in death or injuries to children. Remedy: Refund Recall date: September 13, 2017 Recall[Read More…]
Medtronic Announces Voluntary Recall of Diabetes Infusion Sets
Silver Spring, Maryland–(ENEWSPF)–September 12, 2017. Medtronic plc (NYSE:MDT) announced today that it has started to inform patients worldwide of a voluntary recall of specific lots of infusion sets used with all models of Medtronic insulin pumps. The recall is related to a certain discontinued component in these infusion sets and[Read More…]
Garden of Life LLC Issues Recall of Baby Organic Liquid Formula
Silver Sprng, Maryland–(ENEWSPF)–September 8, 2017. Garden of Life, LLC, is issuing a voluntary precautionary recall of its new supplement for infants, Baby Organic Liquid, because the product, as labeled, includes directions for use that may be misinterpreted. The company is concerned that if not administered precisely following the labeled instructions,[Read More…]
Lucky Mart Inc. Issues Voluntary Nationwide Recall Of Piyanping Anti-Itch Lotion
Silver Spring, Maryland–(ENEWSPF)–August 31, 2017. Lucky Mart Inc. is voluntarily recalling lots C14005, C16001 and C16002 of Piyanping Anti-Itch Lotion to the consumer level. The product was manufactured using the active pharmaceutical ingredient dexamethasone rather than hydrocortisone. Dexamethasone is not listed as an ingredient in the labeling. Dexamethasone is a[Read More…]
Grand BK Corp. Issues Allergy Alert on “California Aloha Mix”
Silver Spring, Maryland–(ENEWSPF)–August 17, 2017. GRAND BK CORP. of Maspeth, New York is recalling its 14 ounce packages of “CALIFORNIA ALOHA MIX” because they may contain undeclared tree nuts (Almonds, Walnuts and Cashews). People who have allergies or severe sensitivity to tree nuts (Almonds, Walnuts and Cashews) run the risk[Read More…]
Amneal Pharmaceuticals Issues Voluntary Nationwide Recall of Lorazepam Oral Concentrate
Dosing Droppers Supplied with the Product May be Misprinted Silver Spring, Maryland–(ENEWSPF)–August 17, 2017. Amneal Pharmaceuticals LLC is voluntarily recalling 13 lots of Lorazepam Oral Concentrate, USP 2mg/mL, to the Consumer level due to a defect in the dropper markings. The Lorazepam Oral Concentrate, USP 2mg/mL, product is packaged with[Read More…]
