Summary Company Announcement Date: March 18, 2022 FDA Publish Date: March 18, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential foreign material contamination Company Name: Continental Mills Brand Name: Brand Name(s) Product Description: Product Description Buttermilk Pancake & Waffle Mix Company Announcement Continental Mills has issued a recall of Kroger…
The Salsa Texan Issues Allergy Alert on Undeclared Wheat Contamination in “Gluten Free Coconut Flour Tortillas”
Summary Company Announcement Date: March 18, 2022 FDA Publish Date: March 18, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared wheat Company Name: The Salsa Texan Brand Name: Brand Name(s) The Salsa Texan Product Description: Product Description Coconut Flour Tortillas Company Announcement The Salsa Texan of Flower Mound, Texas is…
FDA Warns Against Use of Renuvion/J-Plasma Device for Certain Aesthetic Procedures: FDA Safety Communication
Date Issued: March 14, 2022 The U.S. Food and Drug Administration (FDA) is warning consumers and health care providers against the use of the Renuvion/J-Plasma device by Apyx Medical for certain aesthetic procedures. Specifically, the FDA is warning against the use for procedures intended to improve the appearance of the skin through dermal resurfacing (a…
Cavendish Farms Issues Allergy Alert on Undeclared Wheat in Original Hash Brown Patties
Summary Company Announcement Date: March 17, 2022 FDA Publish Date: March 17, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared wheat Company Name: Cavendish Farms Corporation Brand Name: Brand Name(s) Cavendish Farms Product Description: Product Description Hash Brown Patties Company Announcement Cavendish Farms Corporation of Dieppe, New Brunswick, Canada, is…
Use and Store At-Home COVID-19 Tests Properly to Avoid Potential Harm: FDA Safety Communication
Date Issued: March 18, 2022 The U.S. Food and Drug Administration (FDA) is alerting people that there is a potential for harm if FDA authorized at-home COVID-19 tests are not used according to the manufacturer’s test instructions. The FDA is also reminding people to keep the tests out of reach from children and pets. …
Celltrion USA Recalls Certain Celltrion DiaTrust COVID-19 Ag Rapid Tests for False Positive Test Results and Unauthorized Shelf Life
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: Celltrion DiaTrust COVID-19 Ag Rapid Test Product Code: 83QKP Lot Numbers: See Recall Database Entry Distribution Dates: June 2, 2021, to December 21, 2021 Devices…
SD Biosensor Recalls STANDARD Q COVID-19 Ag Home Tests That Are Not Authorized, Cleared, or Approved by the FDA and May Give False Results
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: SD Biosensor STANDARD Q COVID-19 Ag Home Test Product Codes and Lot Numbers: See recall database entry Distribution Dates: August 26, 2021 to January 30,…
Celltrion USA Recalls Celltrion DiaTrust COVID-19 Ag Rapid Tests for False Positive Test Results and Unauthorized Shelf Life
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: Celltrion DiaTrust COVID-19 Ag Rapid Test Product Code: 83QKP Lot Numbers: See Recall Database Entry Distribution Dates: June 2, 2021, to December 21, 2021 Devices…
LuSys Laboratories, Inc Recalls COVID-19 Antigen Tests (Nasal/Saliva) and COVID-19 IgG/IgM Antibody Tests Because They Are Not Authorized, Cleared, or Approved by the FDA
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 Names: COVID-19 Antigen Test (Saliva) COVID-19 Antigen Test (Nasal) COVID-19 IgG/IgM Antibody Test Product Codes: Distribution Dates: June 1, 2020 to July 21, 2021 Devices Recalled…
Florida Dietary Supplement Salesman Sentenced for Conspiring to Defraud the FDA and Conspiring to Distribute Anabolic Steroids
U.S. Department of Justice FOR IMMEDIATE RELEASEFriday, March 11, 2022 A Florida man who led sales for a sports and dietary supplements retailer was sentenced today to 51 months in prison for conspiring to defraud the U.S. Food and Drug Administration (FDA) and conspiring to distribute anabolic steroids. According to court documents and evidence presented at…