Philips Allura Xper — Class II medical device recall Z-2587-2023
Ongoing recall by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., reported 2023-09-20. A damaged foot switch may cause instances where no or only intermittent x-ray radiation initiation is possible
| Recall number | Z-2587-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., Best, Netherlands |
| Recall initiated | 2023-08-15 |
| Classified | 2023-09-14 |
| Reported by FDA | 2023-09-20 |
| Quantity | 19,115 systems |
| Model numbers | 708032, 708034, 708036, 708037, 708038, 722001, 722002, 722003, 722005, 722006, 722008, 722010, 722011, 722012, 722013, 722015, 722019, 722020, 722022, 722023, 722025, 722026, 722027, 722028, 722029 and 25 more |
Product
Philips Allura Xper, Allura Centron, Allura CV, Azurion, UNIQ Clarity, and MultiDiagnost-Eleva systems
Reason for recall
A damaged foot switch may cause instances where no or only intermittent x-ray radiation initiation is possible.
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-2587-2023. 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.