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 21081–21100 of 38,428 recalls
Recalled Item: Artis zee biplane
The Issue: After the Large Display returns from power save
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniDiagnost Classic X-ray system Angiographic and Diagnostic
The Issue: The fixation of the upper and lower tilt
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee ceiling
The Issue: After the Large Display returns from power save
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor
The Issue: After the Large Display returns from power save
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q.zen biplane
The Issue: After the Large Display returns from power save
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor MN
The Issue: After the Large Display returns from power save
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prima Plus ¿4.1 x 11.5mm Implant
The Issue: Mislabeling
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hobbs Bronchial Cytology Brushes
The Issue: Device was marketed for uses outside the 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jasper Vektor
The Issue: The firm has received 106 complaints of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.