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 24821–24840 of 38,428 recalls
Recalled Item: Por fullct fem st 20x200mm
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 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: Fem IM Nail 15mmdx44cm
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 20x200mm
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Segmental vss bowed 19x190mm
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 16mmdx50cm
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 16mmdx48cm
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 16x200mm
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 14mmdx48cm right
The Issue: Zimmer Biomet Inc. initiated a field action on
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tibial IM Nail 15mmdx44cm
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: Stryker SmartLife Large Aseptic Housing (7126-120-000)
The Issue: Stryker Instruments issued a notice of correction for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYFRECATOR 2000 HANDPIECE SHEATH
The Issue: For over a year, the Accessory Packages in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths
The Issue: For over a year, the Accessory Packages in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths
The Issue: For over a year, the Accessory Packages in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths
The Issue: For over a year, the Accessory Packages in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile Handpiece Sheaths
The Issue: For over a year, the Accessory Packages in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Stryker Visum¿ LED Surgical Lighting system is intended to
The Issue: The potential hazard that can arise for the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.