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 20561–20580 of 38,428 recalls

June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3 (Stitching Patient Support) 712025

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Upgrades (Stitching Patient Support) 712083

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712082

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 Chest / Emergency (Stitching Patient Support) 712029

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: EasyDiagnost Eleva DRF

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 (Stitching Patient Support) 712225

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost R90 (Stitching Patient Support) 709030

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Classic

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Stryker GmbH

Recalled Item: Stryker T2 ANKLE ARTHRODESIS NAIL RIGHT 10MMX200MM Item Number: 1819-1020S

The Issue: Incomplete seal on the Tyvek lid may compromise

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost Dual Detector (Stitching Patient Support) 712022

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4 Flex / Value (Stitching Patient Support) 712028

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated
June 27, 2018· Philips Medical Systems Gmbh, DMC

Recalled Item: DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031

The Issue: The hook does not securely hold the footplate

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

Class II — Potential Health HazardTerminated