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 17241–17260 of 38,428 recalls
Recalled Item: Kit BD Max Enteric Viral Panel RUO
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max StaphSR
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 1 USA
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit EXT Enteric Bacterial Panel
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Check-Points CPO IVD EU
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Enteric Viral Panel EU Catalog # 443985
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK TNA 2
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 1 EU LUO
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max MRSA
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Vaginal Panel
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 2 EU LUO
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max StaphSR
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max CT/GC/TV
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Cdiff EU
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max GC RT PCR Assay
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Enteric Parasite Panel EU
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max ExK DNA 2 USA
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max Enteric Bacterial Panel EU
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kit BD Max MRSA XT
The Issue: The foil bags containing extraction tubes for BD
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: U3-3 Solar Blue
The Issue: Power supply unit (PS-SBL) not correctly labeled, and
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.