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 36421–36440 of 38,428 recalls

January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx100 GUIDING CATH MC Product Code: GCB51000000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx90 GUIDING CATH HH Product Code: GHH60900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx90 GUIDING CATH MCV Product Code: GCB60900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GHH51000000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx90 GUIDING CATH MPD Product Code: GMD50900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx100 GUIDING CATH MP Product Code:GMD51000000 Intended for use

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMC61000000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx90 GUIDING CATH MCV Product Code: GCB50900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx90 GUIDING CATH MPC Product Code: GMC50900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx100 GUIDING CATH ST Product Code: GST51000000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx90 GUIDING CATH S2 Product Code: GSM50900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH HH Product Code: GHH61000000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx90 GUIDING CATH HH Product Code: GHH50900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx100 GUIDING CATH S2 Product Code: GSM51000000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx90 GUIDING CATH MPC Product Code: GMC60900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx90 GUIDING CATH ST Product Code: GST50900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MPD Product Code: GMD60900000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MC Product Code: GCB61000000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated
January 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GMC51000000 Intended for

The Issue: Sterility of device may be compromised due to

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

Class II — Potential Health HazardTerminated