Philips DuraDiagnost X-Ray system — Class II medical device recall Z-1251-2015
Terminated recall by Philips Medical Systems, Inc., reported 2015-03-18. Improper installation of Tube arm, and Wall stand may cause it to fall down, Improper installation of table ma
| Recall number | Z-1251-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems, Inc., Andover, MA, United States |
| Recall initiated | 2015-01-23 |
| Classified | 2015-03-06 |
| Reported by FDA | 2015-03-18 |
| Terminated | 2016-06-07 |
| Countries outside the US | AR, AU, CH, CL, CN, CO, DE, EC, ES, FR, GB, HU, ID, IQ, KW, MY, PL, SA, SI, TR |
| Quantity | 71 units |
| Serial numbers | SN120001, SN120002, SN120003, SN130001, SN130002, SN130003, SN130004, SN130005, SN130006, SN130007, SN130009, SN130010, SN130011, SN130012, SN130013, SN130014, SN130015, SN130016, SN130017, SN130018, SN130019, SN130020, SN130021, SN130022, SN130023 and 42 more |
| Model numbers | 712210, 712211 |
Product
Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211
Reason for recall
Improper installation of Tube arm, and Wall stand may cause it to fall down, Improper installation of table may cause it to float.
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-1251-2015. 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.