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 5761–5780 of 38,428 recalls

March 12, 2024· Philips North America Llc

Recalled Item: Intera 1.0T Omni/Stellar

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: GYROSCAN ACS-NT

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Achieva XR

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Achieva Nova-Dual

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Ingenia 1.5T CX

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Ingenia Elition S

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Explorer/Nova Dual

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Ingenia Elition X

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Enterprise 1.5T

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Intera CV

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Achieva 1.5T Conversion

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Intera 1.0T Power/Pulsar

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Evolution Upgrade 3.0T

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: SmartPath to dStream for 1.5T

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Achieva 3.0T for PET

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: MR 5300

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Ingenia Ambition X

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Intera 1.5T Power/Pulsar

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: Intera 0.5T Standard

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing
March 12, 2024· Philips North America Llc

Recalled Item: SmartPath to dStream for XR and 3.0T

The Issue: Patient support table floor plate may be incorrectly

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

Class II — Potential Health HazardOngoing