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 34061–34080 of 38,428 recalls

December 24, 2013· ICU Medical, Inc.

Recalled Item: 11" Smallbore Bifuse Ext Set w/1.2 Micron Filter

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 8" Smallbore Pentafuse Ext Set w/5 NanoClave"

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 120" 10 Drop Primary Set w/2 BCV-CLAVE¿

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: NanoClave Connector

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.33 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 5" Smallbore Ext Set w/MicroClave¿ T-Connector

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.24 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 6" (15 cm) Appx 0.26 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.29 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 17 cm (7'') Ext Set w/NanoClave¿

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 10" (25 cm) Appx 0.41 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 184 cm (72") Smallbore Bifuse Ext Set w/2 NanoClave¿

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 30" (76 cm) Appx 3.7 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 10" (25 cm) Appx 2.9 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 11" Smallbore Bifuse Ext Set w/1.2 Micron Filter

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 5" (13 cm) Appx 0.23 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 6.5" (16.5 cm) Appx 0.30 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 13" Smallbore Ext Set w/4 Gang 4-Way Stopcock w/Baseplate

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 7" (18 cm) Appx 0.26 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated
December 24, 2013· ICU Medical, Inc.

Recalled Item: 87" (221 cm) Appx 2.9 ml

The Issue: ICU Medical is recalling certain lots of the

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

Class II — Potential Health HazardTerminated