FDA Med Watch
FDA Med Watch
The feed below is an automatic RSS feed from the FDA website.
- Potential Risks with Certain Uses of Radiofrequency (RF) Microneedling – FDA Safety Communication
- Alert: Automated Impella Controller Correction due to Cybersecurity Issue from Abiomed
- FDA Approves Labeling Changes that Include a Boxed Warning for Immune Effector Cell-associated Enterocolitis Following Treatment with Ciltacabtagene Autoleucel (CARVYKTI, Janssen Biotech, Inc.)
- Trividia Health, Inc. Initiates Voluntary Recall of Limited Number of TRUE METRIX® Blood Glucose Meters
- What is a Medical Device Recall?
- Update on Alert: Infusion Set Performance Issue from BD
- Recall and Alert Resources
- What is an Early Alert?
- Update on Alert: Infusion Set Performance Issue from BD
- Blood and Plasma Warming Device Correction: 3M Company Issues Correction for Ranger Blood/Fluid Warming System
- Endoscopic Aspiration Needle Recall: Olympus Removes Certain ViziShot 2 FLEX (19G) Needles Due to Potentially Deformed A-traumatic Tips
- Endoscopic Aspiration Needle Recall: Olympus Removes Certain ViziShot 2 FLEX (19G) Needles Due to Potentially Deformed A-traumatic Tips
- Blood and Plasma Warming Device Correction: 3M Company Issues Correction for Ranger Blood/Fluid Warming System
- Early Alert: Automated Impella Controller Purge Retainer Fixation Issue from Abiomed
- Early Alert: Automated Impella Controller Purge Retainer Fixation Issue from Abiomed