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 2401–2420 of 38,428 recalls
Recalled Item: Meridian Bioscience ImmunoCard STAT! Crypto/Giardia Test Kits
The Issue: A single lot of the ImmunoCard STAT! Crypto/Giardia
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX S NEEDLE OUS
The Issue: Boston Scientific has identified that IceSeedTM CX needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX NEEDLE OUS
The Issue: Boston Scientific has identified that IceSeedTM CX needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX S NEEDLE US
The Issue: Boston Scientific has identified that IceSeedTM CX needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IceSeed 1.5 CX NEEDLE US
The Issue: Boston Scientific has identified that IceSeedTM CX needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head
The Issue: The associated product labeling does not adequately provide
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head
The Issue: The associated product labeling does not adequately provide
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head
The Issue: The associated product labeling does not adequately provide
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head
The Issue: The associated product labeling does not adequately provide
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Biomet Ceramic Head
The Issue: The associated product labeling does not adequately provide
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn Connex Vital Signs Monitor (CVSM):
The Issue: There were customer reports of devices which experienced
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn CONNEX Accessory Power Management Stand:
The Issue: There were customer reports of devices which experienced
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Welch Allyn CP150 Electrocardiograph:
The Issue: There were customer reports of devices which experienced
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phasor Drill
The Issue: Drill for use in neurosurgical procedures may have
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC Elite: The OEC Elite mobile C-arm is intended to
The Issue: OEC Elite and OEC 3D Mobile C-Arms Exceeding
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 3D
The Issue: OEC Elite and OEC 3D Mobile C-Arms Exceeding
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESTATION 650C A1
The Issue: GE HealthCare has become aware that certain Carestation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESTATION 620 A2
The Issue: GE HealthCare has become aware that certain Carestation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare CARESTATION 750 A2
The Issue: GE HealthCare has become aware that certain Carestation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Carestation 650 SE
The Issue: GE HealthCare has become aware that certain Carestation
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.