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 20841–20860 of 38,428 recalls
Recalled Item: UNI-CP
The Issue: Use of the impacted product may cause a
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANSYS MLP/DLP
The Issue: Use of the impacted product may cause a
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 45 mm Articulating Vascular/Medium Loading Unit with Tri-Staple
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling system
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 60 mm Articulating Medium/Thick Reload with Tri-StapleTechnology
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Large QWIX
The Issue: Use of the impacted product may cause a
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 60 mm Articulating Vascular/Medium Loading Unit with Tri-Staple
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 60 mm Extra Thick Black Articulating Reload with Tri-Staple Technology
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 45 mm Extra Thick Black Articulating Reload with Tri-Staple Technology
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVANSYS TTC
The Issue: Use of the impacted product may cause a
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo GIA 45mm Curved Tip Articulating Vascular/Medium Reload with Tri-Staple
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Staple 2.0 Black Intelligent Reload for use with Signia stapling
The Issue: Device may be missing a sled component. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads
The Issue: The recalling firm has received a higher than
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads
The Issue: The recalling firm has received a higher than
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads
The Issue: The recalling firm has received a higher than
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads
The Issue: The recalling firm has received a higher than
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LFIT Anatomic CoCr Femoral Heads
The Issue: The recalling firm has received a higher than
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.