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 24661–24680 of 38,428 recalls

March 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM Product Number:

The Issue: for the cutting blade to detach from

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

Class II — Potential Health HazardTerminated
March 15, 2017· Avid Medical, Inc.

Recalled Item: Vacutainer Tubes Vacutainer tubes are intended for clinical laboratory...

The Issue: Avid Medical Inc has received a complaint was

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

Class II — Potential Health HazardTerminated
March 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM Product Number:

The Issue: for the cutting blade to detach from

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

Class II — Potential Health HazardTerminated
March 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9MM Product Number:

The Issue: for the cutting blade to detach from

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

Class II — Potential Health HazardTerminated
March 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10.5MM Product Number:

The Issue: for the cutting blade to detach from

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

Class II — Potential Health HazardTerminated
March 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6MM Product Number:

The Issue: for the cutting blade to detach from

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

Class II — Potential Health HazardTerminated
March 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 5.5MM Product Number:

The Issue: for the cutting blade to detach from

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

Class II — Potential Health HazardTerminated
March 15, 2017· Smith & Nephew, Inc.

Recalled Item: Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11.5MM Product Number:

The Issue: for the cutting blade to detach from

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated
March 15, 2017· Intuitive Surgical, Inc.

Recalled Item: STAPLER

The Issue: Intuitive Surgical has become aware and further investigation

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

Class II — Potential Health HazardTerminated