FDA Med Watch
FDA Med Watch
The feed below is an automatic RSS feed from the FDA website.
- Correction Alert: Olympus Updates Use Instructions for Ligating Device
- Early Alert: Glucose Monitor Sensor Issue from Abbott Diabetes Care
- Recall Alert: Glycar SA Removes Pericardial Patch
- Correction Alert: Becton Dickinson Updates Use Instructions for BD Alaris Pump Issue
- Recall Alert: Baxter Permanently Removes Life2000 Ventilation System
- Recall Alert: BALT USA Removes MEGA Ballast Distal Access Platform
- Recall Alert: Max Mobility/Permobil Removes All SpeedControl Dials Used with SmartDrive MX2+ Power Assist Devices
- Early Alert: Large Volume Pump Primary Administration Set Reverse Flow Issue from Fresenius Kabi
- Correction Alert: Medline Industries, LP Updates Use Instructions for Medline Kits Containing Flexicare BritePro Solo Fiber Optic Laryngoscope Handles
- Recall Alert: Intersurgical Inc Removes i-View Video Laryngoscope
- Alert: Medline Industries, LP Removes Certain Sterile Medline Convenience Kits
- Alert: NOxBOX Ltd. Issues Correction for NOxBOXi Nitric Oxide Delivery System Due to Rapid Command Input Issue
- Alert: NOxBOX Ltd. Issues Correction for NOxBOXi Nitric Oxide Delivery System Due to Risk for Nitric Oxide Dosing Fluctuations
- Alert: Update to Use Instructions for B Braun Hemodialysis Blood Tubing Set
- Alert: Siemens Healthineers Issues Correction for 3 Tesla MRI Systems