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 1741–1760 of 38,428 recalls

July 3, 2025· Philips Ultrasound, Inc

Recalled Item: D5cwc Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: Transducer C10-3v Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: L12-3 Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: Mini Multi TEE Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: S4-1 Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: V6-2 Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: C9-4 Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: L12-5 50 Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: V9-2 Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: XL14-3 Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: X8-2t Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: C9-3io Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: L11-3 Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: OMNI III TEE Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Orascoptic Surgical Acuity

Recalled Item: Orascoptic Superior Visualization Custom loupes with Dragonfly frames

The Issue: Due to complaints, loupe nose pads containing nickel

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

Class II — Potential Health HazardOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: D2TCD Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: C5-2 Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: L15-7IO TRANSDUCER Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: X7-2t Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing
July 3, 2025· Philips Ultrasound, Inc

Recalled Item: C9-5ec Transducer Probe

The Issue: To provide clarification and labelling to define the

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

Class III — Low RiskOngoing