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 4561–4580 of 38,428 recalls
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed
The Issue: Fractures and breakages in packaging trays and Tyvek
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed
The Issue: Fractures and breakages in packaging trays and Tyvek
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Everest Bipolar Cutting Forceps are intended to be passed
The Issue: Fractures and breakages in packaging trays and Tyvek
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX500 with L.x and M.x
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX400 with L.x and M.x
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter PST 500 U
The Issue: Baxter Healthcare Corporation is issuing an Urgent Medical
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX450 with L.x and M.x
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliVue Patient Monitor MX550 with L.x and M.x
The Issue: Philips lntelliVue Patient Monitors MX400/450/500/550 Shipped or Upgraded
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Semi-rigid suction liners labeled as follows: a) SEMI RIGID
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline convenience kits containing semi-rigid suction liners labeled as...
The Issue: Due to reported adverse events, Medline Industries, LP
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.