FDA Med Watch
FDA Med Watch
The feed below is an automatic RSS feed from the FDA website.
- Par Health Issues Voluntary Nationwide Recall of Two Lots of Brevital® Sodium 500 mg/vial CIV (Methohexital Sodium for Injection, USP) Due to the Presence of Particulate Matter
- Early Alert: Diagnostic Ultrasound System Issue from Philips Ultrasound
- Nova Biomedical® Announces Global Medical Device Correction for StatStrip® Glucose Hospital Meter
- Infusion Set Recall: BD and CareFusion 303, Inc. Remove BD Alaris Pump Infusion Sets
- IV Tubing Set Correction: ICU Medical Updates Use Instructions for IV Tubing Sets
- Breathing Circuit Recall: Draeger Removes VentStar Resus Neo Hoses
- Greenwich Rx Issues Voluntary Nationwide Recall of Compounded Glutathione Due to Elevated Endotoxin Levels
- 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