ProxiDiagnost N90 — Class II medical device recall Z-0280-2024
Ongoing recall by Philips North America Llc, reported 2023-11-15, distributed nationwide. Potential for units suspended on the ceiling to fail and fall.
| Recall number | Z-0280-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America Llc, Cambridge, MA, United States |
| Recall initiated | 2023-09-21 |
| Classified | 2023-11-08 |
| Reported by FDA | 2023-11-15 |
| Distributed | Nationwide (US) |
| Quantity | 101 units |
| UPC / GTIN / UDI-DI | 00884838085619, 00884838103221 |
| Serial numbers | 10000008, 10000010, 10000011, 10000013, 10000015, 10000017, 10000018, 10000020, 10000021, 10000023, 10000024, 10000025, 10000026, 10000028, 10000030, 10000031, 10000035, 10000036, 10000037, 10000040, 10000043, 10000045, 10000050, 10000051, 10000052 and 73 more |
| Model numbers | 706100, 706110 |
Product
ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system
Reason for recall
Potential for units suspended on the ceiling to fail and fall.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0280-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
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.