Philips North America Llc recalls DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images

Recalled November 15, 2023 · FDA recall Z-0275-2024 · Philips North America

Hazard

Potential for units suspended on the ceiling to fail and fall. · FDA Class II

Units

33 units

Sold at

Nationwide distribution.

Description

Potential for units suspended on the ceiling to fail and fall.

Product

DigitalDiagnost C90 Flex/Value/Chest/ER, 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 →