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 17521–17540 of 38,428 recalls
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 126 Units Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Lithium HeparinN (LH) 37 USP Units Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer LH (Lithium Heparin) 34 I.U. Plus Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Lithium HeparinN (LH) 56 USP Units Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 56 Units Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 83 Units Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer LH (Lithium Heparin) 68 I.U. Plus Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Lithium HeparinN 75 USP Units Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer LH (Lithium Heparin) 102 I.U. Plus Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Lithium HeparinN (LH) 158 USP Units Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer PST Gel and Lithium HeparinN (LH) 65 Units Blood Collection Tubes
The Issue: False elevation of carboxyhemoglobin (COHb) results have been
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee floor MN
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 dTC
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 FA
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 dMP
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: Artis zee ceiling
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 dBA
The Issue: A tolerance issue in the power supply of
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.