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 25901–25920 of 38,428 recalls
Recalled Item: ADJUSTABLE DRILL GUIDE
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: 8.0CM Heavy Duty Medium 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: GREEN ROTATING CRANIOTOME
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 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: 14CM 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: 12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 45 degree Contra Angle 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: 90 DEG RIGHT ANGLE ATTACH
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: IMRI CRANI-A 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: eMax2 Motor Assembly 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: 16CM MIN INVASIVE ATTACH
The Issue: Supplied Directions for Use (DFU) did not contain
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AL-III-DISS Adapter 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: 11CM 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: eMax2 Hybrid Hand Control 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: 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: Electronic Foot Control with Direction Switch 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: 10.5cm QD Angle 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: IMRI MOTOR 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.