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 2841–2860 of 38,428 recalls

January 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1)

The Issue: The forceps have been used in ways not

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

Class II — Potential Health HazardOngoing
January 31, 2025· Aesculap Inc

Recalled Item: Numerous models of nonsterile hemostatic forceps: (1)

The Issue: The forceps have been used in ways not

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: SIGNA MR355

The Issue: For certain MR systems, a scan can be

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: Paradigm and MMT-715

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: Paradigm insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: Paradigm insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· DeRoyal Industries Inc

Recalled Item: DeRoyal Tubing

The Issue: Due to the inner diameter of the suction

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

Class II — Potential Health HazardOngoing
January 31, 2025· Medtronic MiniMed, Inc.

Recalled Item: MiniMed insulin pump

The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G,

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

Class II — Potential Health HazardOngoing
January 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: Brivo MR355

The Issue: For certain MR systems, a scan can be

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

Class II — Potential Health HazardOngoing
January 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: SIGNA Creator

The Issue: For certain MR systems, a scan can be

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

Class II — Potential Health HazardOngoing
January 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: SIGNA MR380

The Issue: For certain MR systems, a scan can be

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

Class II — Potential Health HazardOngoing
January 31, 2025· GE Healthcare (China) Co., Ltd.

Recalled Item: Optima MR360

The Issue: For certain MR systems, a scan can be

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

Class II — Potential Health HazardOngoing