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 1901–1920 of 38,428 recalls
Recalled Item: Medline Convenience Kits
The Issue: Affected convenience kits contain BD ChloraPrep Clear -
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Convenience Kits
The Issue: Affected convenience kits contain BD ChloraPrep Clear -
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bridge to Life EasiSlush
The Issue: The firm issued a field safety notice after
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular
The Issue: Due to packaging discrepancy with the incorrect tibial
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EMPOWR Dual Mobility" Product Name: EMPOWR Acetabular
The Issue: Due to packaging discrepancy with the incorrect tibial
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
The Issue: Due to defects (bubbles/voids) identified during standard finished
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680
The Issue: Lots from Generation (GEN) 15 of VITROS Chemistry
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PARTIAL NEPHRECTOMY - ROBOTIC. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROBOTIC PROSTATECTOMY PACK. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HVI CARDIAC ROBOT PACK. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GENERAL ROBOTIC PACK. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GYN ROBOTIC PACK. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAP CHOLE PACK. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PACK GENERAL ROBOTIC. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAVH PACK. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPIC PROSTATECTOMY. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DAVINCI TRUCUSTOM BUNDLE. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPIC GYN. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LAPAROSCOPIC TRAY. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROBOTIC URO/GYN PACK. Medical convenience kit.
The Issue: CLEARIFY VISUALIZATION SYSTEM was inadvertently resterilized in kits,
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.