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 17541–17560 of 38,428 recalls
Recalled Item: AXIOM Artis dFA
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis dTA
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee multi
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis TA
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis dFC
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis BA
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis BC
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis FC
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis dBC
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis MP
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis TC
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXIOM Artis dFC
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee biplane MN
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZOLL AED PRO Automated External Defibrillator Product Usage: The AED
The Issue: There is a potential for the device to
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StemPro¿ MSC SFM CTS"
The Issue: Component was not tested by the supplier for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CTSTM Essential 8 Medium
The Issue: Component was not tested by the supplier for
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Human Assayed Multi-Sera Level 2
The Issue: The RX Series control target and range value
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.