MobileDiagnost wDR motorized portable diagnostic X-ray systems — Class II medical device recall Z-1040-2015
Terminated recall by Sedecal S.A., reported 2015-02-11, distributed nationwide. Reports of unexpected movement.
| Recall number | Z-1040-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sedecal S.A., Algete, N/A, Spain |
| Recall initiated | 2014-08-06 |
| Classified | 2015-02-02 |
| Reported by FDA | 2015-02-11 |
| Terminated | 2016-06-22 |
| Distributed | Nationwide (US) |
| Quantity | 283 systems |
| Serial numbers | 12000166, 13000046, 13000047, 13000048, 13000049, 13000053, 13000054, 13000055, 13000056, 13000057, 13000058, 13000060, 13000064, 13000067, 13000070, 13000071, 13000075, 13000077, 13000078, 13000079, 13000085, 13000090, 13000092, 13000093, 13000094 and 254 more |
Product
MobileDiagnost wDR motorized portable diagnostic X-ray systems.
Reason for recall
Reports of unexpected movement.
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-1040-2015. 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.