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.

38,428 total recalls
0 this month

Showing 20001–20020 of 38,428 recalls

August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-P180

The Issue: The attachment of non-Olympus accessories to the bronchoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchofiberscope BF-P40

The Issue: The attachment of non-Olympus accessories to the bronchoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Ultrasonic Bronchoscope BF-UC180F

The Issue: The attachment of non-Olympus accessories to the bronchoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-MP60

The Issue: The attachment of non-Olympus accessories to the bronchoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-1T180

The Issue: The attachment of non-Olympus accessories to the bronchoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchofiberscope BF-40

The Issue: The attachment of non-Olympus accessories to the bronchoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-1T40

The Issue: The attachment of non-Olympus accessories to the bronchoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovidescope BF-1T240

The Issue: The attachment of non-Olympus accessories to the bronchoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-P160

The Issue: The attachment of non-Olympus accessories to the bronchoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-3C160

The Issue: The attachment of non-Olympus accessories to the bronchoscope

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System

The Issue: The back cap separates from the body of

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System

The Issue: The back cap separates from the body of

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System

The Issue: The back cap separates from the body of

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System

The Issue: The back cap separates from the body of

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite 23 GA Vit Cutter

The Issue: The back cap separates from the body of

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite 20 GA Vit Cutter

The Issue: The back cap separates from the body of

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System

The Issue: The back cap separates from the body of

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System

The Issue: The back cap separates from the body of

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite Vision Enhancement System

The Issue: The back cap separates from the body of

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated
August 8, 2018· Bausch & Lomb Inc

Recalled Item: Bausch + Lomb Stellaris Elite 25 GA Vit Cutter

The Issue: The back cap separates from the body of

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardTerminated