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 Affected Serial Numbers for Z-800 (UDI-DI: 00814377102006) 800242 801925 802867 900875 901058 901089 901101 901126…
Intra-Operative Positioning System Guidewire Recall: Centerline Biomedical Removes Certain IOPS Guidewires due to Delamination
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 Device Name Model Number UDI-DI Lot Number IOPS Guidewire ATW-2 H01035 00843152102051 2404-2005 What to…
Liquid Bicarbonate Concentrate Recall: Nipro Removes MedicaLyte Liquid Bicarbonate Concentrate due to Contamination
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 MedicaLyte Liquid Bicarbonate Concentrate – 45x Proportioning (BC+201) Unique Device Identifier (UDI)/Model: 00817411022824 What to Do…
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…
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…
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…
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…