Radiography 7300 C — Class II medical device recall Z-0466-2026
Ongoing recall by Philips Medical Systems DMC GmbH, reported 2025-11-19, distributed nationwide. Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through J
| Recall number | Z-0466-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems DMC GmbH, Hamburg, Germany |
| Recall initiated | 2025-10-01 |
| Classified | 2025-11-07 |
| Reported by FDA | 2025-11-19 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, BH, CA, CH, CL, DE, DK, EE, ES, FI, FR, GB, GH, HR, ID, IL, IQ, IT, JO, KR, KW, LT, LV, NL, NO, NZ, PA, PH, PL, PT, SA, SE, SG, ZA |
| Quantity | 284 units |
| UPC / GTIN / UDI-DI | 00884838116016 |
| Serial numbers | 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 and 249 more |
| Model numbers | 712037 |
Product
Radiography 7300 C; Model Number: 712037;
Reason for recall
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.
Machine access
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Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.