This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program. The FDA has become aware of a potentially high-risk device issue. The FDA will keep the public informed and update this web page as significant new information becomes available. Affected Product The FDA is aware that Trokamed has issued a…
Lidl Recalls Taste of Deutschland Buttered Vegetables Due to Undeclared Milk Allergens
Summary Company Announcement Date: December 20, 2024 FDA Publish Date: December 20, 2024 Product Type: Food & Beverages Vegetable Products Allergens Reason for Announcement: Recall Reason Description Undeclared milk Company Name: Lidl US Brand Name: Brand Name(s) Taste of Deutschland Product Description: Product Description Frozen Buttered Vegetables, Carrots, Peas, Cauliflower, & Corn Company Announcement ARLINGTON,…
Endo USA, Inc. Issues Voluntary, Nationwide Recall of Adrenalin® Chloride Solution (EPINEPHrine Nasal Solution, USP) Due to the Potential for Administration Errors
Summary Company Announcement Date: December 20, 2024 FDA Publish Date: December 20, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Product is an unapproved drug. Company Name: Endo, Inc. Brand Name: Brand Name(s) Par Pharmaceutical Product Description: Product Description Adrenalin® Chloride Solution (EPINEPHrine nasal solution, USP) Company Announcement MALVERN, PA, December 20, 2024…
Recall of Jose Madrid Salsa Chipotle Con Queso
Summary Company Announcement Date: December 20, 2024 FDA Publish Date: December 20, 2024 Product Type: Food & Beverages Gravy/Sauces Allergens Reason for Announcement: Recall Reason Description Undeclared Yellow 5 and Yellow 6 Company Name: Jose Madrid Salsa Brand Name: Brand Name(s) Jose Madrid Product Description: Product Description Chipotle Con Queso Salsa Company Announcement Jose Madrid…
Orgain Issues Voluntary Allergy Alert on Possible Undeclared Peanut Residue in a Single Batch of 30G Protein Organic Plant Based Powder – Chocolate 2.01lb
Summary Company Announcement Date: December 19, 2024 FDA Publish Date: December 19, 2024 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Product may contain undeclared peanut Company Name: Orgain Brand Name: Brand Name(s) Product Description: Product Description 30g Plant Protein Complete Protein Powder – Chocolate Company Announcement Orgain of Irvine, California…
Shoppers-Plaza Issues Voluntary Nationwide Recall of Fouzee Sugarlin Herbal Formula Due To Presence Of Undeclared Metformin And Glyburide
Summary Company Announcement Date: December 16, 2024 FDA Publish Date: December 18, 2024 Product Type: Drugs Reason for Announcement: Recall Reason Description Product contains undeclared Metformin and Glyburide Company Name: Shoppers-Plaza Brand Name: Brand Name(s) Product Description: Product Description SugarLin Herbal Formula Herbal Dietary Supplement Company Announcement FOR IMMEDIATE RELEASE – December 16, 2024 –…
Lexington Doctor Sentenced for Engaging in International Money Laundering Scheme and Importing Illegal and Misbranded Drugs
Department of JusticeU.S. Attorney’s OfficeDistrict of Massachusetts FOR IMMEDIATE RELEASETuesday, December 17, 2024 Defendant falsified documents to obtain drugs from Hong Kong that are not FDA-approved BOSTON – A Lexington, Mass. doctor was sentenced yesterday in federal court in Boston for an international money laundering scheme involving importing illegal, misbranded drugs. Rahim Shafa, 66, was…
Fruit Juice Manufacturing Company and its Former President Plead Guilty to Food Safety Crimes
Department of JusticeOffice of Public Affairs FOR IMMEDIATE RELEASEThursday, December 19, 2024 The former president and primary owner of the now-closed fruit juice manufacturer Valley Processing Inc. (VPI) in Sunnyside, Washington, pleaded guilty this week to two misdemeanor charges related to the manufacture and sale of tainted fruit juice products in violation of federal food…
Implantable Marker Recall: Hologic Removes BioZorb 3D Bioabsorbable Markers due to Risk for Patient Complications
This recall involves removing devices from where they are used or sold. The FDA has identified this recall as the most serious type. This device may cause serious injury or death if you continue to use it. Affected Product Product Names: BioZorb Marker and BioZorb LP Marker Product Codes: NEU Product Part Numbers: F0405 BioZorb…
Former Nurse Pleads Guilty to Tampering with Medication
Department of JusticeU.S. Attorney’s OfficeEastern District of Kentucky FOR IMMEDIATE RELEASEWednesday, December 18, 2024 FRANKFORT, Ky. – A Lexington, Ky., woman, Abigail Hall, 51, pleaded guilty on Monday, before U.S. District Judge Gregory Van Tatenhove, to tampering with a consumer product. According to her plea agreement, between January 2023 and August 2023, Hall worked…