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 22601–22620 of 38,428 recalls
Recalled Item: MINOR DRESSING CHANGE TRAY
The Issue: Convenience Kit contains a PVP Prep Pad, received
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXCISION TRAY
The Issue: Convenience Kit containing components to assist practitioner with
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WOUND CARE KIT
The Issue: Convenience Kit containing components to assist practitioner with
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INCISION & DRAINAGE TRAY or KIT
The Issue: Convenience Kit contains a PVP Prep Pad, received
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUBING CHANGE KIT
The Issue: Convenience Kit contains a PVP Prep Pad, received
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WOUND CLOSURE TRAY - FACIAL
The Issue: Convenience Kit containing components to assist practitioner with
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SKIN STAPLE REMOVER
The Issue: Convenience Kit contains a PVP Prep Pad, received
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PEDIATRIC IV & IV START KIT
The Issue: Convenience Kit containing components to assist practitioner with
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST. CHRISTOPHER'S SECUREMENT SET
The Issue: Convenience Kit contains a PVP Prep Pad, received
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgical punch
The Issue: Surgical punches are being recalled due to potential
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Curved Circular Staplers Product Usage: Staplers have application...
The Issue: There is a potential for the devices to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radial Osteotome Blade
The Issue: The expiration date provided on the label is
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensicare Green Surgical Glove
The Issue: open seal on top portion of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tissu-Trans Filtron 1000 Catalog Number 3-TT-FILTRON 1000. Used for fat
The Issue: breach of sterility of the packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrasound Transducer
The Issue: The ultrasound probe may not have adequate protection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARVEST TERUMOBCT
The Issue: Certain lots of the Harvest Graft Delivery System
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARVEST(R) TERUMOBCT
The Issue: The patient labels included in the BMAC system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARVEST(R) TERUMOBCT
The Issue: The patient labels included in the BMAC system
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 22701
The Issue: The Better Bladder device provided as part of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BEQ-TOP 22702 ECC W/HMOD 30000
The Issue: The Better Bladder device provided as part of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.