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 26801–26820 of 38,428 recalls
Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe
The Issue: The packaging seal may contain a crease. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution Bags
The Issue: The packaging seal may contain a crease. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece with 5mm x 32cm Length Probe
The Issue: The packaging seal may contain a crease. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Trumpet Handpiece only
The Issue: The packaging seal may contain a crease. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece without Probe for Single Solution or
The Issue: The packaging seal may contain a crease. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Suction Irrigation Handpiece Y-Tubing set
The Issue: The packaging seal may contain a crease. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CORE¿ Trumpet Handpiece with 5mm x 32cm Length Probe
The Issue: The packaging seal may contain a crease. The
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intermediate carton label reads in part as: "Bard-Parker***Stainless Steel...
The Issue: After receiving a complaint the firm disclosed that
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 9025TRU Arterial Blood Gas (ABG) Kit is used to
The Issue: Arterial Blood Gas (ABG) Kit- Missing Safety Component
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-TEK TWIST D 40X90MM 30MM Cann 12MM Rnd
The Issue: Zimmer Biomet initiated a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V-TEK TWIST D 3.5X90MM 30MM Can 12MM Rnd
The Issue: Zimmer Biomet initiated a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWIST DR 25X95MM Cann 12MM Thd 30MM AO
The Issue: Zimmer Biomet initiated a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWIST D 28X150MM CBS 45 Cann 14 MM AO
The Issue: Zimmer Biomet initiated a voluntary recall of the
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchron Systems No Foam DxC ( No. B64130) affects
The Issue: Beckman Coulter has identified an incompatibility between No
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer RoboRack 25ul
The Issue: Filter Tips molded incorrectly and may not seal
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Adaptor for Small Battery Drive and Small Battery Drive II.
The Issue: There was a potential for the Adaptor and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adaptor for Small Battery Drive and Small Battery Drive II.
The Issue: There was a potential for the Adaptor and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roadrunner Uniglide Hydrophilic Wire Guide
The Issue: coating contamination with glass particles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perioscopy Sheath: Part number: 1008
The Issue: The Perioscopy Sheaths are currently provided with a
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synovis VASCU-GUARD Peripheral Vascular Patch in the following sizes and
The Issue: Baxter is issuing a safety alert in response
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.