Summary Company Announcement Date: June 12, 2025 FDA Publish Date: June 12, 2025 Product Type: Food & Beverages Allergens Reason for Announcement: Recall Reason Description Potential or Undeclared Allergen – Sulfites Company Name: Turkana Food Inc. Brand Name: Brand Name(s) Product Description: Product Description Dried Apricots Company Announcement Turkana Food Inc. Kenilworth, NJ is recalling…
Anesthesia Breathing Circuit Kit Correction: Draeger, Inc. Updates Use Instructions for VentStar Flex and Anesthesia Circuit Kits Due to Cracks in Hose That May Cause Inadequate Ventilation
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 Part No. Product Name UDI-DI Potential Affected Lots MP00355 VentStar Flex 220 04048675248996 All Lot…
Bornstein Seafoods Inc Recalls Cooked & Peeled Ready-To-Eat Coldwater Shrimp Meat Because of Possible Health Risk
Summary Company Announcement Date: June 10, 2025 FDA Publish Date: June 10, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Listeria monocytogenes Company Name: Bornstein Seafoods Inc. Brand Name: Brand Name(s) Bornstein Seafoods Product Description: Product Description Coldwater Shrimp Meat Company Announcement June 10, 2025,…
Hofood99 Inc Recalls Enoki Mushroom Due to Possible Health Risk
Summary Company Announcement Date: June 11, 2025 FDA Publish Date: June 11, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Listeria monocytogenes Company Name: Hofood99 Inc. Brand Name: Brand Name(s) Product Description: Product Description Enoki Mushrooms Company Announcement Hofood99 Inc of Brooklyn, NY 11231 is recalling its…
Medtronic Announces Voluntary Recall of Select Newport™ HT70 and Newport™ HT70 Plus Ventilators and Certain Related Newport™ Service Parts
Summary Company Announcement Date: June 11, 2025 FDA Publish Date: June 11, 2025 Product Type: Medical Devices Reason for Announcement: Recall Reason Description Device & Drug Safety – Potential Defect Company Name: Medtronic Brand Name: Brand Name(s) Newport™ Product Description: Product Description Newport™ HT70 and HT70 Plus ventilators and certain related service parts Company Announcement…
Infusion Pump Recall: Infusion Pump Intermittent Connection Issue from Smiths Medical
This recall involves correcting certain 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 Smiths…
P. East Trading Corp Distributors Issues Alert on Uneviscerated ‘Salted Smoked Split Herring’ Due to Potential Clostridium Botulinum Contamination
Summary Company Announcement Date: June 10, 2025 FDA Publish Date: June 10, 2025 Product Type: Food & Beverages Foodborne Illness Reason for Announcement: Recall Reason Description Potential Foodborne Illness – Clostridium Botulinum Company Name: P. East Trading Corp Distributors Brand Name: Brand Name(s) Product Description: Product Description Uneviscerated Salted Smoked Split Herring Company Announcement P….
Infusion Pump Correction: Baxter Updates Instructions for Use for Novum IQ Large Volume Pump due to Potential for Underinfusion
This recall involves updating instructions for using 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 following the updated instructions. Affected Product Affected Product:…
Infusion Pump Recall: Infusion Pump Thermal Damage Issue from Smiths Medical
This recall involves correcting certain 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 Smiths Medical…
August Egg Company Recalls Shell Eggs Because of Possible Health Risk
Summary Company Announcement Date: June 06, 2025 FDA Publish Date: June 06, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Salmonella Company Name: August Egg Company Brand Name: Brand Name(s) Multiple brand names Product Description: Product Description Brown cage free and brown certified organic eggs Company Announcement August Egg Company of…