Philips North America Llc recalls DigitalDiagnost C90 Release 3.1, used to acquire, process, s
Recalled Product
DigitalDiagnost C90 Release 3.1, used to acquire, process, store, display and export digital radiographic images.
Hazard / Issue
Potential for units suspended on the ceiling to fail and fall.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Model No. 712026; Serial No. SN14000197 & SN14000260.
View official government recall
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