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Philips North America Llc recalls DigitalDiagnost C90, Model No. 712034 and 712035
Recalled July 5, 2023 · FDA recall Z-2042-2023 · Philips North America
Hazard
There is a software login in issue that may prevent the user from logging in. · FDA Class II
Units
58
Sold at
Distribution in US: AZ, GA, IN, IA, MN, NE, NH, OH, TX OUS distribution to Australia, Chile, China, Malta, Namibia, New Zealand, Oman, Panama, Qatar, Suriname, United Kingdom
Description
There is a software login in issue that may prevent the user from logging in.
Product
DigitalDiagnost C90, Model No. 712034 and 712035
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →