Philips North America, LLC recalls ProxiDiagnost N90
Recalled Product
ProxiDiagnost N90
Hazard / Issue
Unexpected increase in peak tube potential (kV) will lead to an increased patient radiation dose.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: All ProxiDiagnost N90 systems are affected.
View official government recall
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