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 20241–20260 of 38,428 recalls
Recalled Item: CE18TOD CONT EPIDURAL TRAY LF
The Issue: The catheter connectors may not stay closed during
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLAMP STYLE CATH. CONNECTOR 18-19 GA- LF
The Issue: The catheter connectors may not stay closed during
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TOD CONT EPIDURAL TRAY LF
The Issue: The catheter connectors may not stay closed during
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TKFPS PERIFIX FX CONT. EPID TRAY-LF
The Issue: The catheter connectors may not stay closed during
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GOVCE18TK ACCU-BLOC PERIFIX KIT
The Issue: The catheter connectors may not stay closed during
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TKFMHDT 17 GA X 4 FULL EPID KIT
The Issue: The catheter connectors may not stay closed during
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CE17TB19C CONT EPIDURAL TRAY
The Issue: The catheter connectors may not stay closed during
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Thread PLGA Full Thread Interference Screw
The Issue: The Gentle Thread PLGA Round Head, 7x20mm and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Thread PLGA Round Head Interference Screw
The Issue: The Gentle Thread PLGA Round Head, 7x20mm and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for:
The Issue: Instructions for Use (IFU) and Surgical Cleaning and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for
The Issue: Instructions for Use (IFU) and Surgical Cleaning and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for
The Issue: Instructions for Use (IFU) and Surgical Cleaning and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Surgical Cleaning Sterilization Protocol for Trilliant
The Issue: Instructions for Use (IFU) and Surgical Cleaning and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for:
The Issue: Instructions for Use (IFU) and Surgical Cleaning and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for
The Issue: Instructions for Use (IFU) and Surgical Cleaning and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for:
The Issue: Instructions for Use (IFU) and Surgical Cleaning and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for
The Issue: Instructions for Use (IFU) and Surgical Cleaning and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for
The Issue: Instructions for Use (IFU) and Surgical Cleaning and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use and Surgical Cleaning and Sterilization Protocol for
The Issue: Instructions for Use (IFU) and Surgical Cleaning and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Beaver Accu-Temp High Temperature Cautery
The Issue: A small number of devices in this lot
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.