Summary Company Announcement Date: February 28, 2022 FDA Publish Date: March 07, 2022 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Consumer complaints regarding Cronobacter sakazakii, Salmonella Newport Company Name: Abbott Brand Name: Brand Name(s) Similac, Alimentum, and EleCare Product Description: Product Description Powder Infant Formula Company Announcement 02.28.2022 EXPANDED:…
Urgent: Torn & Glasser Recalls Sprouts Farmer Market Dark Chocolate Covered Cherries 12 Oz. Because of Undeclared Almond Allergen
Summary Company Announcement Date: March 04, 2022 FDA Publish Date: March 04, 2022 Product Type: Food & Beverages Snack Food Item Allergens Reason for Announcement: Recall Reason Description Undeclared almonds Company Name: Torn & Glasser Brand Name: Brand Name(s) Sprouts Farmers Market Product Description: Product Description Dark Chocolate Covered Cherries Company Announcement Torn & Glasser…
The Third Synthesis Inc Issues Allergy Alert on Undeclared Egg, Milk, and Wheat Allergen Statement
Summary Company Announcement Date: February 28, 2022 FDA Publish Date: March 03, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared egg, wheat, milk allergen Company Name: Chicago Sweet Connection Baker Brand Name: Brand Name(s) Chicago Sweet Connection Bakery Product Description: Product Description Coffee cake and paczkis varieties Company Announcement The…
B. Braun Medical Inc. Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride for Injection USP 250ML in Excel Due to Fluid Leakage or Low Fill Volume
Summary Company Announcement Date: March 02, 2022 FDA Publish Date: March 03, 2022 Product Type: Drugs Reason for Announcement: Recall Reason Description Fluid leakage and low fill volume may cause a lack in sterility Company Name: B. Braun Medical Inc. Brand Name: Brand Name(s) B. Braun Medical Inc. Product Description: Product Description 0.9% Sodium Chloride…
Do Not Use Certain Celltrion DiaTrust COVID-19 Tests: FDA Safety Communication
March 2, 2022 Update: The FDA updated this Safety Communication to clarify that the DiaTrust COVID-19 Ag Rapid Tests in the green and white packaging are a product of Celltrion Healthcare. Date Issued: March 1, 2022 The U.S. Food and Drug Administration (FDA) is warning people not to use certain Celltrion USA Inc. DiaTrust COVID-19…
Do Not Use SD Biosensor STANDARD Q COVID-19 Ag Home Tests: FDA Safety Communication
Date Issued: March 1, 2022 The U.S. Food and Drug Administration (FDA) is warning people not to use the SD Biosensor Inc. STANDARD Q COVID-19 Ag Home Test. The test is not authorized, cleared, or approved by the FDA for distribution or use in the United States. The FDA is concerned about the risk of…
COVID-19 Test Basics
Image Español 简体中文 한국어 Tagalog Việt COVID-19 testing plays a critical role in the fight against the virus. Understanding COVID-19 tests, including the different types of tests and their uses, and the types of samples the tests use, is key to making an informed decision that meets your needs. Types of Tests There are different…
Do Not Use Certain ACON Flowflex COVID-19 Tests: FDA Safety Communication
Date Issued: March 1, 2021 The U.S. Food and Drug Administration (FDA) is warning people not to use certain ACON Laboratories COVID-19 tests. People should not use the ACON Laboratories test named “Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing)” that is packaged in a dark blue box (see image below). This test has not been authorized,…
Dried Plums Recall Information-Alli and Rose LLC Snak Yard Dried Plums/Saladitos
Summary Company Announcement Date: February 15, 2022 FDA Publish Date: February 24, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description potential to be contaminated with lead Company Name: Alli and Rose LLC Brand Name: Brand Name(s) Product Description: Product Description Dried Plums/ saladitos Company Announcement IDENTIFYING FEATURESBarcode: 810019600821Item code: 1516905 Dates…
FDA Advisory Panel Recommendations on Lifelong Surveillance and Long-Term Postmarket Data Collection for Patients with AAA Endovascular Aortic Repair – Letter to Health Care Providers
The U.S. Food and Drug Administration (FDA) is emphasizing to physicians and other health care providers the importance of lifelong surveillance, including imaging, for patients with abdominal aortic aneurysm (AAA) endovascular aortic repair (EVAR). Regular imaging surveillance, within 30-days of EVAR and annually thereafter, may help identify adverse events such as endoleaks, device migration, loss…