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 28341–28360 of 38,428 recalls
Recalled Item: Single Lumen Pressure Monitoring Sets and Trays The subject sets
The Issue: A manufacturing process may lead to catheter tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Femoral Artery Pressure Monitoring Catheter Sets and Trays The subject
The Issue: A manufacturing process may lead to catheter tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single Lumen Central Venous Catheter Sets and Trays The subject
The Issue: A manufacturing process may lead to catheter tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Artery Pressure Monitoring Catheter Sets and Trays The subject
The Issue: A manufacturing process may lead to catheter tip
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMPLANT
The Issue: Information specific to the 3.7 mmD and 4.1
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ET-20 Anesthesia Extension Tubes
The Issue: Firm was notified of a potential product defect
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Left Medial Tibial Trial Tray Size
The Issue: Zimmer Biomet is conducting a medical device field
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Partial Knee System Right Medial Tibial Trial Tray Size
The Issue: Zimmer Biomet is conducting a medical device field
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.