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Philips North America, LLC recalls Poly G Integris H5000, System code 72246
Recalled March 25, 2020 · FDA recall Z-1491-2020 · 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
1
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
Poly G Integris H5000, System code 72246
Manufacturer(s)
Philips North America, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →