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 19981–20000 of 38,428 recalls

August 8, 2018· Olympus Corporation of the Americas

Recalled Item: Bronchovideoscope BF-XP160F

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: Rhino Laryngo scope ENF-VT2

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-240

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 F-1TQ180

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-UC160F-OL8

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 F-1T160

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-P240

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-XT160

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: Bronchofibercope BF-6C240

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-Q180

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-Q180-AC

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-XP40

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-XP60

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-160

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-XT40

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: Airway Mobilescope MAF-TM

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-1T60

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-P60

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-3C40

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-MP160F

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