Philips North America Llc recalls Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray Sy
Recalled Product
Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
Hazard / Issue
Potential for collimator to fall as a result of incorrect installation.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: REF 712214; UDI: (01)00884838064751(21); Serial No. SN170009, SN170010, SN180072, SN180020 200037, SN160061, SN180075, 200089, SN180045, SN160096.
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