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 24801–24820 of 38,428 recalls
Recalled Item: Fem IM Nail 14mmdx48cm left
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx38cm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental malefemale taper
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xl por st 24.0x220mm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental fluted stem
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 15mmdx50cm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Por fullct fem st 18x200mm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xl por st 25.5x220mm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx44cm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx42cm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 15mmdx46cm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 15mmdx48cm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Por fullct fem st 15x200mm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx46cm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 14mmdx50cm right
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 16mmdx40cm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fem IM Nail 14mmdx50cm left
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.