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 28141–28160 of 38,428 recalls
Recalled Item: Product 34 consists of all product under product code: JWH
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 59 consists of all product under product code: JWH
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 10consists of all product under product code HWC
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 65 consists of all product under product code: KTT
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 64 consists of all product under product code: JDI
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 14 consists of all product under product code HSB
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 62 consists of all product under product code: LPH
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 19 consists of all product code: JDI and same
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 35 consists of all product under product code: JWH
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 67 consists of all product under product code: JDI
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 54 consists of all product under product code: JWH
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 1 consists of all product under
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 37 consists of all product under product code: HSB
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 27 consists of all product under product code: HSB
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 7 consists of all products under product code HWC
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 8 consists of all products under product code HWC
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 3 consists of all products under product code JDI
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 15 consists of all product code JDI
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 56 consists of all product under product code: HWC
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 42 consists of all product under product code: HSB
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.