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Philips North America Llc recalls DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images.
Recalled November 15, 2023 · FDA recall Z-0272-2024 · Philips North America
Hazard
Potential for units suspended on the ceiling to fail and fall. · FDA Class II
Units
13 units
Sold at
Nationwide distribution.
Description
Potential for units suspended on the ceiling to fail and fall.
Product
DigitalDiagnost 4 Chest/Emergency, 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 →