The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Name: Cobalt XT, Cobalt, and Crome Implantable Cardioverter Defibrillators (ICDs) and Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) Model Numbers (See recall database entry for more information): Cobalt…
Kraft Heinz is announcing a voluntary recall of Capri Sun Wild Cherry Flavored Juice Drink Blend Beverages Due to Potential for Chemical Contaminants
Summary Company Announcement Date: August 12, 2022 FDA Publish Date: August 16, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential for Clean-In-Place (CIP) solution to have entered the product stream Company Name: Kraft Heinz Brand Name: Brand Name(s) Kraft Heinz Product Description: Product Description Capri Sun Wild Cherry Flavored Juice…
The Gluten Free Bar Issues Allergy Alert on Undeclared Cashew in The GFB 1.2oz Dark Chocolate Coconut Bites
Summary Company Announcement Date: August 16, 2022 FDA Publish Date: August 16, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared cashews Company Name: The Gluten Free Bar Brand Name: Brand Name(s) Product Description: Product Description Dark Chocolate coconut bites Company Announcement The Gluten Free Bar of Grand Rapids, MI is…
French Executive Admits Making False Statements to FDA to Fraudulently Obtain Control of Pharmaceutical Product
Department of JusticeDistrict of New Jersey FOR IMMEDIATE RELEASEFriday, August 12, 2022 NEWARK, N.J. – A French national and executive of a pharmaceutical company admitted making false statements to gain control of the rights to sell a weight-loss drug in the United States, U.S. Attorney Philip R. Sellinger announced today. Alain Bouaziz, 69, a French citizen…
Fifth Season Issues Allergy Alert on Undeclared Dairy and Eggs in Crunchy Sesame Salad Kit
Summary Company Announcement Date: August 14, 2022 FDA Publish Date: August 14, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared eggs and milk Company Name: Fifth Season Brand Name: Brand Name(s) Fifth Season Product Description: Product Description Crunchy sesame salad kit Company Announcement Fifth Season announced today that it is…
King’s Hawaiian® Issues Voluntary Recall of Pretzel Slider Buns, Pretzel Hamburger Buns and Pretzel Bites Due to the Recall of an Ingredient from Supplier Lyons Magnus
Summary Company Announcement Date: August 12, 2022 FDA Publish Date: August 13, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Due to the potential for microbial contamination, including Cronobacter sakazakii and Clostridium botulinum Company Name: King’s Hawaiian Brand Name: Brand Name(s) King’s Hawaiian Product Description: Product Description Pretzel Slider Buns, Pretzel…
Consumer Protection Issues Food Safety Warning for EZ Noble Sushi EZ Noble Sushi is voluntarily recalling the products, which contained unlabeled allergens
Summary Company Announcement Date: August 11, 2022 FDA Publish Date: August 12, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Unlabeled eggs, milk and wheat Company Name: EZ Noble Sushi Brand Name: Brand Name(s) EZ Noble Sushi Product Description: Product Description Sushi products Government Agency Partner Announcement AUGUST 11, 2022 —…
At-Home COVID-19 Antigen Tests-Take Steps to Reduce Your Risk of False Negative: FDA Safety Communication
Date Issued: August 11, 2022 Perform repeat, or serial testing following a negative result on any at-home COVID-19 test, whether or not you have symptoms. The U.S. Food and Drug Administration (FDA) is advising people to perform repeat, or serial, testing following a negative result on any at-home COVID-19 antigen test, to reduce the risk…
Becton Dickinson Recalls Intraosseous Needle Set Kits, Intraosseous Manual Driver Kits, and Intraosseous Powered Drivers for Issues That May Cause Delayed Treatment Delivery
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Name: BD Intraosseous Needle Set Kits, BD Intraosseous Manual Driver Kits, BD Intraosseous Powered Drivers Product Codes: See recall database entry Devices Recalled in the U.S.:…
Lyons Magnus Expands Voluntary Recall to Include Additional Nutritional and Beverage Products Due to the Potential for Microbial Contamination
Lyons Barista Style Sweet Cream Frappé Base12ct/32 fl oz cartons 045796100893 10045796100890 5131 08/08/2022 6131 08/09/2022 Almond Non-Dairy Beverage12ct/32 fl oz cartons 045796101654 10045796101651 0302 10/27/2022 0531 09/12/2022 0602 11/26/2022 1231 08/14/2022 1302 10/28/2022 1602 11/27/2022 2231 08/15/2022 2302 10/29/2022 2602 11/28/2022 3102 10/10/2022 3231 08/16/2022 3602 11/29/2022 4102 10/11/2022 4602 11/30/2022 5602 12/01/2022 9431…