This recall involves removing certain 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. This is an update to an Early Alert; the affected products and recommendations have not changed. Affected…
IQ Produce LCC. Recalls Enoki Mushrooms Because of Possible Health Risk
Summary Company Announcement Date: May 13, 2026 FDA Publish Date: May 14, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Product found positive for Listeria monocytogenes Company Name: IQ Produce LCC Brand Name: Brand Name(s) IQ Produce LCC Product Description: Product Description Enoki Mushrooms 150g package Company Announcement IQ…
HH Fresh Trading. Recalls TW Enoki Mushrooms 150g Because of Possible Health Risk
Summary Company Announcement Date: May 13, 2026 FDA Publish Date: May 14, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Product found positive for Listeria monocytogenes Company Name: HH Fresh Trading Brand Name: Brand Name(s) HH Fresh Trading Product Description: Product Description Enoki Mushrooms 150g Company Announcement HH Fresh…
Terra Medi LLC Recalls Karagounis Bros – Hellas Meze Golden Smoked Whole Herring Due to Improper Evisceration
Summary Company Announcement Date: May 13, 2026 FDA Publish Date: May 14, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Product is an uneviscerated fish with potential for Clostridium botulinum contamination Company Name: Terra Medi LLC Brand Name: Brand Name(s) Hellas Meze Product Description: Product Description Hellas Meze Golden…
Sun Pharmaceutical Industries, Inc. (Sun Pharma) Initiates Voluntary U.S. Nationwide Recall of DOXOrubicin Hydrochloride Liposome Injection 50mg/25 mL Due To Potential Presence of Glass Particles
Summary Company Announcement Date: May 13, 2026 FDA Publish Date: May 13, 2026 Product Type: Drugs Reason for Announcement: Recall Reason Description Presence of glass particles Company Name: Sun Pharmaceutical Industries, Inc. Brand Name: Brand Name(s) Product Description: Product Description DOXOrubicin Hydrochloride Liposome Injection 50mg/25 mL Company Announcement FOR IMMEDIATE RELEASE MUMBAI, INDIA and PRINCETON,…
Fly By Jing Issues Voluntary Recall of Creamy Sesame Noodles Due to Potential Cross-Contact with Peanuts
Summary Company Announcement Date: May 12, 2026 FDA Publish Date: May 13, 2026 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Potential Peanut Contamination Company Name: Fly by Jing Brand Name: Brand Name(s) Fly by Jing Product Description: Product Description Fly By Jing Creamy Sesame Noodles, single packs (NET WT 38…
Pharmacal Issues Nationwide Recall of MG217 Multi-Symptom Treatment Cream & Skin Protectant Eczema Cream Due to Microbial Contamination
Summary Company Announcement Date: May 08, 2026 FDA Publish Date: May 12, 2026 Product Type: Drugs Reason for Announcement: Recall Reason Description Contaminated with Staphylococcus aureus. Company Name: Pharmacal Brand Name: Brand Name(s) Product Description: Product Description Multi-symptom Treatment Cream & Skin Protectant Eczema Cream, 6oz tube Company Announcement – May/8/2026- Jackson, WI, Pharmacal is…
Convenience Kit Recall: AVID Medical Removes Convenience Kits Containing Namic RA Syringes
This recall involves removing certain 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. This is an update to an Early Alert; the affected products and recommendations for what to do…
Sizing Catheter Recall: Cook Medical Removes Various Centimeter Sizing Catheters
This recall involves removing certain 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. The affected products and recommendations for what to do with the devices below have not changed. Affected…
Pacemaker Correction: Boston Scientific Issues Correction for ACCOLADE Pacemakers and CRT-Ps
This recall involves correcting devices, and does not involve removing them 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 without correction. Affected Product The FDA is aware that Boston Scientific…