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 20941–20960 of 38,428 recalls

May 10, 2018· Life Technologies, Corp.

Recalled Item: Gibco Dulbecco's Modified Eagle Medium (DMEM)

The Issue: It has been determined that the fill port

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

Class II — Potential Health HazardTerminated
May 10, 2018· Life Technologies, Corp.

Recalled Item: Gibco Dulbecco's Modified Eagle Medium (DMEM)

The Issue: It has been determined that the fill port

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

Class II — Potential Health HazardTerminated
May 10, 2018· Life Technologies, Corp.

Recalled Item: Gibco RPMI 1640 Medium

The Issue: It has been determined that the fill port

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

Class II — Potential Health HazardTerminated
May 10, 2018· Anika Therapeutics, Inc.

Recalled Item: Hyalomatrix

The Issue: Hyalomatrix products are susceptible to degradation as a

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Manual)

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Manual)

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microtargeting" Depth Stop Adapter

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Motorized) Distributed by Medtronic

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Lead Adapter for microTargeting" Drive

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Distributed by Medtronic

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Manual) Distributed by Medtronic

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Lead Adapter for STar" Drive

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" Drive System Distributed by Medtronic

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Motorized)

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· FHC, Inc.

Recalled Item: microTargeting" STar" Drive System (Motorized)

The Issue: The FHC Depth Stop Adapter may cause damage

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

Class II — Potential Health HazardTerminated
May 10, 2018· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: RS - TANDEM 5F DL BIOFLO MIDLINE

The Issue: A component of the kits might contain unsafe

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

Class II — Potential Health HazardTerminated