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 28161–28180 of 38,428 recalls
Recalled Item: Product 43 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 4 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 16 consists of all product under poduct code: KWY
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 46 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 69 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 30 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 60 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 53 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 63 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 70 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 66 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 20 consists of all prod oct under poduct code:
The Issue: As a result of the insufficient sealer calibration
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product 22 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 13 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 71 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 40 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 47 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 49 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 26 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 41 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.