Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.
Showing 2801–2820 of 39,430 recalls
PIE Medical Imaging B.V.
When fenestrated analysis with clock measurements is started in diagnostic bioimaging software (intended to measure/visualize cardiovascular structures) and the 12h position of a single clock is changed, other clock measurements are not updated relative to the new 12h position which may cause stent graft fenestrations at incorrect position, which may lead to blood flow disruption and tissue damage
Remel, Inc
The products may contain surface and subsurface contamination of Listeria monocytogenes.
ICU Medical, Inc.
ICU Medical identified two sequences of programming events and alarm interactions that may cause the user interface to become unresponsive.