Global Medicines Program
Newsletter Archive
Newsletter archive:
FDA MEDWATCH NEWSFEED
- Update: Do Not Use BioZorb Marker Implantable Radiographic Marker Devices: FDA Safety Communication
- 2024 Medical Device Recalls
- Hologic, Inc. Recalls BioZorb Marker Due to Complications with Implanted Devices
- Catheter Correction: Boston Scientific Updates Use Instructions for POLARx and POLARx FIT Cryoablation Balloon Catheters due to Higher than Anticipated Number of Reports of Atrio-Esophageal Fistula