medical Class II Updated 2025-04-23

Philips North America Llc recalls Philips DXR System, DuraDiagnost 4.1. Stationary X-Ray Syste

Recalled Product

Philips DXR System, DuraDiagnost 4.1. 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 712203; UDI: (01)00884838095205(21); Serial No. 220025, 210023, 220171, 230103, 230152.
View official government recall

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