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 25881–25900 of 38,428 recalls
Recalled Item: 19cm Attachment
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autolube-III with Foot Guard Product Usage: Pneumatic system
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11.0cm Long Attachment Product Usage: Pneumatic system
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autolube-III with Irrigation Product Usage: Pneumatic system
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5.0cm Short Attachment
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large Craniotome Product Usage: Pneumatic system
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8cm QD Angle Attachment
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13.5CM ANGLE ATTACHMENT
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 26.65CM ATTACHMENT
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bearing Sleeve
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autolube-III with 20ft hose Product Usage: Pneumatic system
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: eMax2 PLUS Product Usage: Electric system
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electronic Foot Control with Direction or Irrigation Switches Product Usage:
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compact Speed Reducer
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.1CM ATTACHMENT
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5cm QD Angle Attachment
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10.5cm Long Attachment
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10.5cm Long Attachment Product Usage: Pneumatic system
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9.4CM MICRO REVISION ATTACH
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTRA ANGLE ATTACHMENT
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.