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 15861–15880 of 38,428 recalls

January 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Set

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Combined Spinal Epidural Catheterization Kit

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: Epidural Catheterization Kit with FlexTip Plus Catheter

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Combined Spinal Epidural Catheterization Kit

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Kit

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Combined Spinal Epidural Catheterization Set

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Combined Spinal Epidural Catheterization Kit

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: FlexTip Plus Epidural Catheterization Set

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated
January 15, 2020· Arrow International Inc

Recalled Item: EPIDURAL CATHETERIZATION KIT

The Issue: There is the potential for various failures with

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

Class II — Potential Health HazardTerminated