FDA Med Watch
FDA Med Watch
The feed below is an automatic RSS feed from the FDA website.
- Disruptions in Availability of Neurosurgical Patties, Sponges, and Strips - Letter to Health Care Providers
- Sizing Catheter Recall: Cook Medical Removes Various Centimeter Sizing Catheters
- Surgical Stapler Reload Recall: Intuitive Surgical Removes 8mm SureForm 30 Gray Reloads
- Trividia Health Correction for TRUE METRIX Blood Glucose Monitoring Systems
- Insulin Pump Recall: Insulet Removes Certain Omnipod 5 Pods
- Early Alert: Thoracic Stent Graft Issue from Bolton Medical
- B. Braun Medical, Inc. Issues Voluntary Nationwide Recall of Lactated Ringer’s Injection, 1L, E7500 Due to the Presence of Particulate Matter in Solution
- Risks of Using TRUE METRIX Blood Glucose Monitoring Systems by Trividia Health: FDA Safety Communication
- Blood Glucose Monitor Recall: Trividia Health Issues Correction for TRUE METRIX Blood Glucose Monitoring Systems
- Early Alert: Arrow International Removes Dialysis Catheter Kits Containing Merit Medical Splittable Sheath Introducers
- Early Alert: Automated Compounding System Issue from Omnicell
- Early Alert: Convenience Kit Issue from Aligned Medical Solutions
- Cranial Drill Recall: Integra LifeSciences Recalls Codman Disposable Perforators Due to Risk of Device Disassembly
- Insulin Pump Correction: Tandem Diabetes Care Issues Correction for Tandem Mobi Insulin Pumps
- Windstone Medical Packaging dba Aligned Medical Solutions Issues Nationwide Recall of Namic Angiographic Rotating Adapter 10CC Control Syringe Placed into the Following Kits; AMS6908E Angio Pack, and AMS6908F Angio Pack