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.
Showing 1701–1720 of 38,428 recalls
Recalled Item: L9-3 Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X7-2 Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C8-5 Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: mC7-2 Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X11-4t Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X6-1 Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C9-3v Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L12-4 Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BP10-5ec Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SCNHD LA L7-4 HDI Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L8-4 Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7.5MHZ Endo Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orascoptic Superior Visualization Phantom Nose Pad Accessory Kit ( nose
The Issue: Due to complaints, loupe nose pads containing nickel
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L10-4LAP Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C10-4ec Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X5-1 Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C8-4v Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VL13-5 Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4-1 Lumify Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4-2 Transducer Probe
The Issue: To provide clarification and labelling to define the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.