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 34161–34180 of 38,428 recalls

December 9, 2013· Synergetics Inc

Recalled Item: 23ga Chandelier Infusion Cannula

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: Stiff 25ga Wide Field Endo Illuminator

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: 27ga ONE-STEP (tm) Endo Illuminator

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: Chandelier Infusion Cannula

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: 25ga Awh Vivid Chandelier

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: Two-Port Vitrectomy (TPV (tm)) Wide Field High Flow End Irrigator

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: 23ga Aspirating Endo Illuminator

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: Stiff 25ga Chow Illuminated Pick (Dull)

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: 23ga Straight Fixed Extended Illuminated Laser Probe

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: 25ga Aspirating Endo Illuminator

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: Endo Illuminator

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: "The Corona" Shielded Wide Field Endo Illuminator

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: 25ga Awh Chandelier

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT & Brilliance iCT SP Computed Tomography X-Ray Systems

The Issue: Patient images exhibited ring artifacts

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: 25ga Mid-Field Endo Illuminator

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: Vivid (tm) Endo Illuminator

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: 25ga Awh Chandelier

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: 23ga Endo Illuminator (Eckardt Trocar Compatible)

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: Standard tubing set

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated
December 9, 2013· Synergetics Inc

Recalled Item: 25ga Wide Field Corona Endo Illuminator

The Issue: Faulty seals on the outer pouch of various,

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

Class II — Potential Health HazardTerminated