Summary Company Announcement Date: January 27, 2026 FDA Publish Date: January 28, 2026 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Undeclared Allergen – Sesame, Wheat Company Name: Koikoi Trading Inc. Brand Name: Brand Name(s) Product Description: Product Description Fish balls Company Announcement Commerce, CA – Koikoi Trading Inc. is recalling…
IKM Recalls Product Because of Possible Health Risk
Summary Company Announcement Date: January 23, 2026 FDA Publish Date: January 23, 2026 Product Type: Food & Beverages Contaminants Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Lead contamination Company Name: IKM Brand Name: Brand Name(s) Product Description: Product Description Metal Cookware Items Company Announcement IKM of San Jose, California is…
Navitas Organics Voluntarily Recalls Select Lots of 8oz Organic Chia Seeds Because of Possible Health Risk
Summary Company Announcement Date: January 23, 2026 FDA Publish Date: January 23, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Salmonella Company Name: Navitas Organics Brand Name: Brand Name(s) Navitas Organice Product Description: Product Description Organic Chia Seeds Company Announcement Navitas Organics is voluntarily recalling…
Early Alert: Insufflation Unit Issue from Olympus
CDRH is issuing this Early Alert to notify the public 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 Olympus has issued a letter to affected customers recommending certain High Flow Insufflation Units…
Early Alert: Wound and Burn Dressing Issue from Integra LifeSciences
CDRH is issuing this Early Alert to notify the public 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 Integra LifeSciences has issued a letter to affected customers recommending all MediHoney Wound and…
Anesthetic Vaporizer Recall: Draeger Removes Vapor 2000 and Vapor 3000 Vaporizers
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. Affected Product The FDA is aware that Draeger has issued a letter to affected customers recommending certain…
Tri-Union Seafoods Identifies Additional Quantities of Recalled Genova® Tuna at Limited Retailers Due to Inadvertent Distribution of Previously Recalled Product
Summary Company Announcement Date: January 16, 2026 FDA Publish Date: January 19, 2026 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential contamination with Clostridium botulinum Company Name: Tri-Union Seafoods Brand Name: Brand Name(s) Product Description: Product Description Yellowfin Tuna Company Announcement El Segundo, CA, January 16, 2026 – Tri-Union…
Early Alert: Broselow Rainbow Tape Issue from AirLife
This communication is a medical device early alert. 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 AirLife has issued a letter to affected customers recommending certain Broselow…
Olympus Expands Voluntary Recall for ViziShot 2 FLEX (19G) EBUS -TBNA Needles
Summary Company Announcement Date: January 16, 2026 FDA Publish Date: January 16, 2026 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Device & Drug Safety – Defect Company Name: Olympus Corporation Brand Name: Brand Name(s) Product Description: Product Description ViziShot 2 FLEX (19G) EBUS -TBNA needles Company Announcement CENTER VALLEY, Pa., (January 16,…
Early Alert: Stent and Electrocautery-Enhanced Delivery System Issue from Boston Scientific
This communication is a medical device early alert. 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 Boston Scientific has issued a letter to affected customers recommending certain…