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 37681–37700 of 38,428 recalls
Recalled Item: LUSTER HIP SZ 3 Packaging: The product was packaged within
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 9 Packaging: The product was packaged within
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 5 Packaging: The product was packaged within
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 10 Packaging: The product was packaged within
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 6 Packaging: The product was packaged within
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 7 Packaging: The product was packaged within
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 4 Packaging: The product was packaged within
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LUSTER HIP SZ 8 Packaging: The product was packaged within
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ULTIMA*LX STM
The Issue: DePuy Orthopaedics, Inc. is issuing a Field Safety
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 13mm UPN Outer Box:
The Issue: Difficulty in extending snare loop from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 11mm UPN Outer Box
The Issue: Difficulty in extending snare loop from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Profile Single-Use Pediatric Snare 27mm UPN Outer Box:
The Issue: Difficulty in extending snare loop from the catheter
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.