Home / Recalls / Medical Devices
Philips North America Llc recalls DigitalDiagnost 4 Flex/Value, used to acquire, process, store, display and export digital radiographic images.
Recalled November 15, 2023 · FDA recall Z-0273-2024 · Philips North America
Hazard
Potential for units suspended on the ceiling to fail and fall. · FDA Class II
Units
92 units
Sold at
Nationwide distribution.
Description
Potential for units suspended on the ceiling to fail and fall.
Product
DigitalDiagnost 4 Flex/Value, 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 →