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 14501–14520 of 38,428 recalls

July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Globus Medical, Inc.

Recalled Item: ALTERA Spacer ALTERA Spacer

The Issue: Specific lots of ALTERA¿ implants have internal components

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

Class II — Potential Health HazardTerminated
July 22, 2020· Smith & Nephew Orthopaedics AG

Recalled Item: POLARSTEM COLLAR Reamer Guide

The Issue: Multiple lots being recalled due to a product

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

Class II — Potential Health HazardOngoing
July 21, 2020· BEYOND WHITE SPA LLC D.B.A. EZYWIPE OF AMERCIA

Recalled Item: Ezycare Face Mask

The Issue: Disposable face masks labeled as non-medical were distributed

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

Class II — Potential Health HazardOngoing
July 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube

The Issue: The electrode insulating material on the Cobra EMG

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

Class II — Potential Health HazardTerminated
July 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 2-Ch EMG ET Tube

The Issue: The electrode insulating material on the Cobra EMG

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

Class II — Potential Health HazardTerminated
July 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-CH EMG ET Tube

The Issue: The electrode insulating material on the Cobra EMG

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

Class II — Potential Health HazardTerminated
July 21, 2020· Neurovision Medical Products Inc

Recalled Item: Cobra x5 1-Ch EMG ET Tube

The Issue: The electrode insulating material on the Cobra EMG

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

Class II — Potential Health HazardTerminated
July 21, 2020· Neurovision Medical Products Inc

Recalled Item: Nerveana x5 RLN Monitoring Kit with Cobra 1-Ch EMG ET Tube

The Issue: The electrode insulating material on the Cobra EMG

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

Class II — Potential Health HazardTerminated