FDA Device recall Z-0466-2026
Radiography 7300 C
- FDA Device
- Class II
- ongoing
- Published 2025-11-19
On 2025-11-19 the FDA classified a Class II recall of Radiography 7300 C by Philips Medical Systems Dmc, citing philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/p….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0466-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-10-01 |
| Published | 2025-11-19 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips Medical Systems Dmc |
| Distribution | US |
Product
Radiography 7300 C; Model Number: 712037;
Reason
Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.
Identifiers
| code_info | Model Number: 712037; UDI-DI: 00884838116016; Serial Numbers: 6, 7, 8, 9, 11, 12, 13, 14, 15, 17, 24860004, 24860006, 2…Model Number: 712037; UDI-DI: 00884838116016; Serial Numbers: 6, 7, 8, 9, 11, 12, 13, 14, 15, 17, 24860004, 24860006, 24860008, 24860009, 24860010, 24860011, 24860012, 24860013, 24860014, 24860015, 24860017, 24860018, 24860019, 24860021, 24860034, 24860036, 24860037, 24860038, 24860039, 24860040, 24860044, 24860045, 24860047, 24860049, 24860051, 24860053, 24860055, 24860056, 24860057, 24860058, 24860059, 24860060, 24860061, 24860062, 24860064, 24860065, 24860066, 24860067, 24860068, 24860069, 24860070, 24860072, 24860073, 24860074, 24860075, 24860076, 24860077, 24860078, 24860079, 24860080, 24860081, 24860082, 24860083, 24860084, 24860085, 24860086, 24860087, 24860088, 24860089, 24860090, 24860091, 24860092, 24860093, 24860094, 24860096, 24860098, 24860099, 24860100, 24860101, 24860102, 24860103, 24860104, 24860105, 24860106, 24860107, 24860108, 24860109, 24860110, 24860111, 24860112, 24860113, 24860115, 24860116, 24860117, 24860118, 24860119, 24860120, 24860121, 24860122, 24860123, 24 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0466-2026%22
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