Philips North America Llc Recall 93200
Description: DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images.
Philips North America Llc Recall 93200 Information
Status | Ongoing |
Mandated? | Voluntary: Firm initiated |
Recall Number | Z-0272-2024 |
Event ID | 93200 |
Event Description | DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export digital radiographic images. |
Product Type | Devices |
Distribution | Nationwide distribution. |
Quantity | 13 units |
Recall Reason | Potential for units suspended on the ceiling to fail and fall. |
Device Classification | 20231115 |
Device 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. |
Center Classification Date | 20231108 |
Recall Initiation Date | 20230921 |
Recalling Firm | Philips North America Llc |
Initial Notification | Letter |
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