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Philips North America Llc recalls DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and export digital radiographic images.
Recalled November 15, 2023 · FDA recall Z-0278-2024 · Philips North America
Hazard
Potential for units suspended on the ceiling to fail and fall. · FDA Class II
Units
2 units
Sold at
Nationwide distribution.
Description
Potential for units suspended on the ceiling to fail and fall.
Product
DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and export digital radiographic images.
Manufacturer(s)
Philips North America Llc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →