Home / Recalls / Medical Devices
Philips North America, LLC recalls MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038
Recalled March 25, 2020 · FDA recall Z-1489-2020 · Philips North America
Hazard
A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible. · FDA Class II
Units
534
Sold at
Nationwide domestic distribution. Foreign distribution worldwide.
Description
A capacitor inside the converter of the Velara X-ray generator may fail after a large number of surges in a short period of time. When this occurs, no image acquisition is possible.
Product
MultiDiagnost Eleva, System codes 722030 722016 722017 708032 708036 708034 708037 708038
Manufacturer(s)
Philips North America, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →