FDA Device recall Z-0280-2024
ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system
- FDA Device
- Class II
- ongoing
- Published 2023-11-15
On 2023-11-15 the FDA classified a Class II recall of ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system by Philips North America, citing potential for units suspended on the ceiling to fail and fall.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0280-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-21 |
| Published | 2023-11-15 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Philips North America |
| Distribution | US |
Product
ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system
Reason
Potential for units suspended on the ceiling to fail and fall.
Identifiers
| code_info | Model No. 706100 & 706110; UDI: (01)00884838085619(21) SN18000019 , (01)00884838085619(21) SN18000019 , (01)00884838085…Model No. 706100 & 706110; UDI: (01)00884838085619(21) SN18000019 , (01)00884838085619(21) SN18000019 , (01)00884838085619(21) SN18000002 , (01)00884838085619(21) 721815121706 , (01)00884838085619(21) 10000015 , (01)00884838085619(21) SN18000014 , (01)00884838085619(21) 20000070 , (01)00884838085619(21) SN19000007 , (01)00884838085619(21) 10000035 , (01)00884838085619(21) 10000011 , (01)00884838085619(21) SN18000021 , (01)00884838085619(21) SN19000002 , (01)00884838085619(21) SN19000001 , (01)00884838085619(21) 10000021 , (01)00884838085619(21) 20000054 , (01)00884838085619(21) SN19000006 , (01)00884838085619(21) SN19000011 , (01)00884838085619(21) SN19000012 , (01)00884838085619(21) SN19000005 , (01)00884838085619(21) 10000051 , (01)00884838085619(21) 20000078 , (01)00884838085619(21) 10000050 , (01)00884838085619(21) 20000045 , (01)00884838085619(21) 10000008 , (01)00884838085619(21) SN19000018 , (01)00884838085619(21) 10000017 , (01)00884838085619(21) 10000045 , (01)00884838085619(2 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0280-2024%22
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