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FDA (Device enforcement)Recalled 2023-09-21class ii

Philips North America Llc: DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images.

Hazard

Potential for units suspended on the ceiling to fail and fall.

Details from the source

Reason for recall: Potential for units suspended on the ceiling to fail and fall. Distribution: Nationwide distribution. Quantity: 13 units Lot/code info: Model No. 712029 & 712033; UDI: (01)00884838074521(21) SN19000272, (01)00884838074521(21) SN19000213 , (01)00884838074521(21) 10001077, (01)00884838074521(21) SN20000097, (01)00884838074521(21) SN16000074, (01)00884838074521(21) SN15000238, (01)00884838074521(21) SN16000075, (01)00884838074521(21) SN15000367, (01)00884838074521(21) SN18000428, (01)00884838074521(21) SN17000318, (01)00884838074521(21) SN18000309, (01)00884838074521(21) SN18000204; Serial No. SN15000409, SN19000272, SN19000213, 10001077, SN20000097, SN16000074, SN15000238, SN16000075, SN15000367, SN18000428, SN17000318, SN18000309, SN18000204.

UPC codes

00884838074521

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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