Carestream Health, Inc. FDA Recalls

3 recalls on file across devices, 0 of them Class I and 3 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
The DRX-Revolution Mobile X-Ray System is a diagnostic mobile x-ray system utilizing digital radiography (DR) technologyClass IIOct 2, 2023There is a potential for unexpected failure of the electrica	There is a potential for unexpected failure of the electrical components within the Carestream Health Inc. gen	Class IIDevices	Oct 2, 2023
DRX Revolution Mobile X-Ray SystemClass IIOct 2, 2023Unexpected failure of electrical components within the CPI g	Unexpected failure of electrical components within the CPI generator.	Class IIDevices	Oct 2, 2023
DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For use in obtaining diagnostic quality radiogrClass IIJan 30, 2023After pressing and releasing the Z-Axis Motorized buttons on	After pressing and releasing the Z-Axis Motorized buttons on the Tube Head Display, the Overhead Tube Crane (O	Class IIDevices	Jan 30, 2023