Medical Device Recalls
This is our largest category by volume. The FDA tracks recalls for an enormous range of medical devices: implants, pacemakers, insulin pumps, surgical tools, blood glucose monitors, X-ray machines, prosthetics, contact lenses, and home health equipment, among many others. We have records dating back to 2005 and add new ones as the FDA publishes them.
Device recalls can happen because of software bugs, manufacturing defects, bacterial contamination, incorrect labeling, or design flaws that lead to inaccurate results or equipment failure. Class I recalls are the most serious and mean the device could cause injury or death.
Showing 7181–7200 of 38,428 recalls
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Spetzler-Malis Bipolar forceps
The Issue: An error was identified on the expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sapphire Infusion Pumps
The Issue: Infusion Pumps with affected software revision may fail
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GS0008 2Y - Burn Pack - STL
The Issue: Medical convenience kit contains Zimmer Dermatome Blades which
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Viewer Workflow Manager
The Issue: When using Universal Viewer or Centricity Universal Viewer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Omega Medical Imaging Elevating Monitor Suspension Systems
The Issue: An actuator separated from the pivot mechanism on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.