FDA Med Watch
FDA Med Watch
The feed below is an automatic RSS feed from the FDA website.
- Angiographic Catheter Recall: Boston Scientific Removes Imager II Angiographic Catheters
- Convenience Kit Correction: Becton Dickinson Issues Correction for Kits and Procedure Trays Containing Recalled Sodium Chloride Ampules
- Heart Pump Controller Recall: Abiomed Removes Automated Impella Controllers
- Early Alert: Ventilator Issue from React Health
- Early Alert: Heart Pump Controller Issue from Abiomed
- Ventilator Recall: CooperSurgical Removes INCA Infant Nasal CPAP Sets
- Convenience Kit Correction: AVID Medical Issues Correction for Kits Containing Huons Sodium Chloride Ampules
- Otsuka ICU Medical LLC Issues Voluntary Nationwide Recall of 0.9% Sodium Chloride Injection, USP Due To a Product Mix-up with 10 mEq Potassium Chloride Injection
- Par Health Issues Voluntary Nationwide Recall of Two Lots of Dexmedetomidine HCl in 0.9% Sodium Chloride Injection Due to the Presence of Particulate Matter
- Nitric Oxide Delivery System Correction: NOxBOX Updates Use Instructions for NOxBOXi Nitric Oxide Delivery System
- Sodium Chloride Flush Recall: Spectra Medical Removes Sodium Chloride Injection USP Ampules
- Esophageal pH Monitoring Capsule Recall: Medtronic and Given Imaging Remove Esophageal pH Monitoring Capsule Delivery Device
- Centric Compounding Issues Nationwide Recall of Glutathione, Myer’s Cocktail, and Tri-Immune Boost Due to Elevated Endotoxin Levels
- Epidural Kit Correction: Medical Action Industries Issues Correction for Epidural Kits Containing Spectra Medical Devices Lidocaine Ampules
- BMC Medical Co., Ltd. Recalls Luna G3 APAP (Model LG3600) with Firmware G3-2.00.76 Due to Firmware Defect