DeECO offers METHANOL FREE Hand Sanitizer in various sizes? Original Post Summary Company Announcement Date: March 07, 2022 FDA Publish Date: March 07, 2022 Product Type: Drugs Reason for Announcement: Product contains methanol Company Name: Tennessee Technical Coatings Corp. Brand Name: Tennessee Technical Coatings Corp. Product Description: Hand Sanitizer Company Announcement Tennessee Technical Coatings Corp.…
Read MoreOriginal Post Summary Company Announcement Date: February 28, 2022 FDA Publish Date: March 07, 2022 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Consumer complaints regarding Cronobacter sakazakii, Salmonella Newport Company Name: Abbott Brand Name: Similac, Alimentum, and EleCare Product Description: Powder Infant Formula Company Announcement 02.28.2022 EXPANDED: Abbott is voluntarily recalling one…
Read MoreOriginal Post Date Issued: March 1, 2022 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…
Read MoreDo not use recalled Similac, Alimentum, and EleCare powdered infant formulas produced in Sturgis, Michigan. Original Post If you use powdered infant formula, be aware certain Similac, Alimentum and EleCare products have been recalled and should not be used. The U.S. Food and Drug Administration (FDA) is investigating consumer complaints of bacterial infections in five…
Read MoreOriginal Post Summary Company Announcement Date: February 17, 2022 FDA Publish Date: February 17, 2022 Product Type: Food & Beverages Reason for Announcement: Consumer complaints regarding Cronobacter sakazakii, Salmonella Newport. Company Name: Abbott Brand Name: Similac, Alimentum, and EleCare Product Description: Powder Infant Formula Company Announcement Abbott (NYSE: ABT) is initiating a proactive, voluntary recall…
Read MoreOriginal Post When a company announces a recall, market withdrawal, or safety alert, the FDA posts the company’s announcement as a public service. FDA does not endorse either the product or the company. Summary Company Announcement Date: February 16, 2022 FDA Publish Date: February 16, 2022 Product Type: Cosmetics, Drugs, Deodorant Reason for Announcement: Presence…
Read MoreOriginal Post Summary Company Announcement Date: February 02, 2022 FDA Publish Date: February 04, 2022 Product Type: Medical Devices Reason for Announcement: illegally imported into the United States Company Name: SD Biosensor, Inc. Brand Name: SD Biosensor, Inc. Product Description: STANDARD Q COVID-19 Ag Home Test Company Announcement January 31, 2022. SD Biosensor, Inc., a…
Read MoreOriginal Post Date Issued: February 4, 2022 The U.S. Food and Drug Administration (FDA) is warning people not to use the E25Bio COVID-19 Direct Antigen Rapid Test. This test has not been authorized, cleared, or approved by the FDA for distribution or use in the United States, and it may include false labeling representing that…
Read MoreOriginal Post For Immediate Release: January 31, 2022 Español Today, the U.S. Food and Drug Administration approved a second COVID-19 vaccine. The vaccine has been known as the Moderna COVID-19 Vaccine; the approved vaccine will be marketed as Spikevax for the prevention of COVID-19 in individuals 18 years of age and older. Key points: Spikevax…
Read MoreOriginal Post Date Issued: January 28, 2022 The U.S. Food and Drug Administration (FDA) is warning people to stop using the Empowered Diagnostics CovClear COVID-19 Rapid Antigen Test and ImmunoPass COVID-19 Neutralizing Antibody Rapid Test. These tests were distributed with labeling indicating they are authorized by the FDA, but neither test has been authorized, cleared,…
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