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…
Infusion Pump Correction: Baxter Issues Correction 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:…
Church & Dwight Co., Inc. Issues Voluntary Nationwide Recall of Zicam® Cold Remedy Nasal Swabs, Zicam® Nasal AllClear Swabs, and Orajel™ Baby Teething Swabs Due to Microbial Contamination
Summary Company Announcement Date: June 06, 2025 FDA Publish Date: June 06, 2025 Product Type: Drugs Reason for Announcement: Recall Reason Description Microbial contamination Company Name: Church & Dwight Co., Inc. Brand Name: Brand Name(s) Zicam® and Orajel™ Product Description: Product Description Cold Remedy Nasal Swabs, Nasal AllClear Swabs, Baby Teething Swabs Company Announcement Church…
Infusion Pump Recall: False Alarm Issue with Infusion Pump 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…
Flexible Tracheostomy Tube Recall: Medtronic Removes Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula Due to Risk for Disconnection of the Flange from the Device Cannula
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 Product Names: Shiley Adult Flexible Tracheostomy Tube with TaperGuard Cuff Reusable Inner Cannula Unique Device…
Tgd Cuts, LLC Initiated Voluntary Recall of Cucumber from Bedner Growers Inc., Which Had the Potential to Be Contaminated with Salmonella
Summary Company Announcement Date: June 04, 2025 FDA Publish Date: June 04, 2025 Product Type: Food & Beverages Reason for Announcement: Recall Reason Description Potential to be contaminated with Salmonella Company Name: TGD Cuts, LLC. Brand Name: Brand Name(s) Multiple brands Product Description: Product Description Fresh cucumbers and salsa and salads containing fresh cucumbers Company…