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 21341–21360 of 38,428 recalls
Recalled Item: OviTex 2S Reinforced BioScaffold 18x22cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 10x20cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 10x12cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 16x20cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 10x20cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 20x20cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 4x8cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 6x10cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 2S Reinforced BioScaffold 20x20cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 6x10cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 20x20cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 16x20cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 18x22cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 16x20cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 10x20cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex Reinforced BioScaffold 10x12cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OviTex 1S Reinforced BioScaffold 18x22cm
The Issue: Degradation of the PGA suture material used in
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T-Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straight Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TN Plate
The Issue: Firm is conducting a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.