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Philips North America Llc recalls DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Recalled June 17, 2026 · FDA recall Z-2354-2026 · Philips North America
Hazard
System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events. · FDA Class II
Units
1 unit
Sold at
US distribution to California.
Description
System was delivered without the required Seismic kit for Wall Stand VS2, which is designed to prevent damage and ensure stability of the Wall Stand VS2 during seismic events.
Product
DigitalDiagnost C90 Flex/Value/Chest/ER. Model Number: 712035.
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →