Summary Company Announcement Date: April 06, 2022 FDA Publish Date: April 07, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared soy and wheat Company Name: Van Law Food Products, Inc. Brand Name: Brand Name(s) Whole Foods Market 365 Product Description: Product Description Organic Creamy Caesar Dressing Company Announcement Van Law…
Pfizer Voluntary Nationwide Recall of Lots of Accuretic (Quinapril HCl/Hydrochlorothiazide), Quinapril and Hydrochlorothiazide Tablets, and Quinapril HCl/Hydrochlorothiazide Tablets Due to N-Nitroso-Quinapril Content
Summary Company Announcement Date: March 22, 2022 FDA Publish Date: March 22, 2022 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of a nitrosamine, N-nitroso-quinapril Company Name: Pfizer Brand Name: Brand Name(s) Accuretic, Greenstone Brand Product Description: Product Description Accuretic™ (quinapril HCl/hydrochlorothiazide); quinapril and hydrochlorothiazide; and quinapril HCl/hydrochlorothiazide tablets Company Announcement NEW YORK,…
Former CEO of Drug Manufacturing Company Charged with Conspiring to Defraud the FDA and Distributing Adulterated Drugs
Department of JusticeU.S. Attorney’s OfficeSouthern District of Florida FOR IMMEDIATE RELEASEMonday, April 4, 2022 Miami, Florida – Raidel Figueroa, the former CEO and co-owner of Pharmatech, LLC, a drug and dietary supplement manufacturer that operated in Broward County, Florida, has made his initial appearance in Fort Lauderdale federal magistrate court to face charges that he…
Use Duodenoscopes with Innovative Designs to Enhance Safety: FDA Safety Communication
Date Issued: April 5, 2022 The U.S. Food and Drug Administration (FDA) is updating the April 2020 Safety Communication to provide new information supporting the transition to fully disposable duodenoscopes and those with disposable components as well as new information on completed postmarket surveillance studies (also known as 522 studies). Given the cleaning concerns and…
UPDATE: Change in Reprocessing Methods with Certain Karl Storz Urological Endoscopes – Letter to Health Care Providers
April 4, 2022 As the U.S. Food and Drug Administration (FDA) continues to evaluate the risk of patient infections and contamination issues associated with reprocessed urological endoscopes, the FDA is aware that the current reprocessing instructions for certain urological endoscopes manufactured by Karl Storz are inadequate and are being changed updated by Karl Storz. The…
Best Brand Consumers Products, Inc. Issues Voluntary Recall of Mickey Mouse Hand Sanitizer Ethyl Alcohol 68% Due to Presence of Methanol and the Mandalorian Hand Sanitizer Ethyl Alcohol 68% Due to the Presence of Benzene
Summary Company Announcement Date: April 01, 2022 FDA Publish Date: April 01, 2022 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of Methanol in Mickey Mouse and Presence of Benzene in The Mandalorian Company Name: Best Brands Consumer Products, Inc. Brand Name: Brand Name(s) Mickey Mouse, The Mandalorian Product Description: Product Description Hand…
B&G Foods Issues Voluntary Allergy Alert for Undeclared Egg and Milk in a Limited Number of Boxes of Back to Nature® Cheddalicious® Cheese Flavored Crackers Mistakenly Containing Animal Shaped Crackers
Summary Company Announcement Date: April 02, 2022 FDA Publish Date: April 02, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Milk and Egg Company Name: B&G Foods Brand Name: Brand Name(s) Back to Nature Product Description: Product Description Cheese Flavored Crackers Company Announcement B&G Foods announced today it is voluntarily…
Two Giant Eagle Stores Recall Cookies Due to Undeclared Milk Allergen
Summary Company Announcement Date: March 31, 2022 FDA Publish Date: April 01, 2022 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Undeclared Milk Company Name: Giant Eagle, Inc. Brand Name: Brand Name(s) Happy Face Cookies Product Description: Product Description Company Announcement Giant Eagle, Inc. has issued a voluntarily recall of “Happy Face…
F&S Medical Supply, DBA Pink Toyz Issues Voluntary Nationwide Recall of Pink Pussycat Capsules Due to the Presence of Undeclared Sildenafil
Summary Company Announcement Date: April 01, 2022 FDA Publish Date: April 01, 2022 Product Type: Drugs Reason for Announcement: Recall Reason Description Undeclared Sildenafil Company Name: F&S Medical Supply, dba Pink Toyz Brand Name: Brand Name(s) F&S Medical Supply, dba Pink Toyz Product Description: Product Description Pink Pussycat Capsules Company Announcement FOR IMMEDIATE RELEASE –…
Unilever Issues Voluntary Nationwide Recall of Suave 24-Hour Protection Aerosol Antiperspirant Powder and Suave 24-Hour Protection Aerosol Antiperspirant Fresh Due to Presence of Slightly Elevated Levels of Benzene
Summary Company Announcement Date: March 30, 2022 FDA Publish Date: March 30, 2022 Product Type: CosmeticsDrugs Deodorant Reason for Announcement: Recall Reason Description Elevated levels of benzene Company Name: Unilever Brand Name: Brand Name(s) Product Description: Product Description Aerosol Antiperspirants Company Announcement March 30, 2022 – Englewood Cliffs, New Jersey– Unilever United States is voluntarily…