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Philips North America, LLC recalls ProxiDiagnost N90
Recalled October 7, 2020 · FDA recall Z-3023-2020 · Philips North America
Hazard
Unexpected increase in peak tube potential (kV) will lead to an increased patient radiation dose. · FDA Class II
Units
71
Sold at
United States
Description
Unexpected increase in peak tube potential (kV) will lead to an increased patient radiation dose.
Product
ProxiDiagnost N90
Manufacturer(s)
Philips North America, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →