Philips DuraDiagnost X-ray systems: DuraDiagnost — Class II medical device recall Z-2322-2017
Terminated recall by Philips Electronics North America Corporation, reported 2017-06-21. Tube arm assembly could fall down due to cracked welding joints
| Recall number | Z-2322-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Electronics North America Corporation, Andover, MA, United States |
| Recall initiated | 2017-05-31 |
| Classified | 2017-06-09 |
| Reported by FDA | 2017-06-21 |
| Terminated | 2018-08-24 |
| Countries outside the US | AE, AR, AU, CH, CL, CN, CO, DE, EC, EG, ES, FR, GB, HU, ID, KW, MX, MY, NL, PE, PL, SA, SI, TR |
| Quantity | 98 sytems |
| Reason classes | packaging |
Product
Philips DuraDiagnost X-ray systems: DuraDiagnost (R1.0, Product Number 712210) DuraDiagnost (R2.0, Product Number 712211) DuraDiagnost (R3.0, Product Number 712211)
Reason for recall
Tube arm assembly could fall down due to cracked welding joints
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-2322-2017. 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.