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 18261–18280 of 38,428 recalls
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CBS 4.5 countersink
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MoniTorr INS1100 INS-1100 CSF Drainage System used with Pole Mount
The Issue: The firm has identified a complaint trend regarding
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LimiTorr INS9020 INS-9020 LIMITORR VOLUME LIMITING EVD 20 ML LimiTorr
The Issue: The firm has identified a complaint trend regarding
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CBS micro
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURIGA XL 4007 BRAZIL SYSTEM Model: M0068FS4007B0 Product Usage: The
The Issue: Certain Auriga consoles may exhibit faster than normal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURIGA 30 BRAZIL SYSTEM UPN: M0068S30B0 Product Usage: The Auriga
The Issue: Certain Auriga consoles may exhibit faster than normal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-TEK"
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURIGA 30 GENERAL SYSTEM UPN: M0068S30G0 Product Usage: The Auriga
The Issue: Certain Auriga consoles may exhibit faster than normal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Sys2.7
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osteofresh arthrodesis drill
The Issue: An investigation identified that the products were possibly
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURIGA XL 4007 GENERAL SYSTEM UPN: M0068FS4007G0 Product Usage: The
The Issue: Certain Auriga consoles may exhibit faster than normal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.