Apollo DRF — Class II medical device recall Z-1429-2017
Terminated recall by Villa Sistemi Medicali S.P.A., reported 2017-03-15, distributed nationwide. Patient fell from the table because the footrest of the device detached from the table top while the patient w
| Recall number | Z-1429-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Villa Sistemi Medicali S.P.A., Buccinasco, N/A, Italy |
| Recall initiated | 2016-12-27 |
| Classified | 2017-03-09 |
| Reported by FDA | 2017-03-15 |
| Terminated | 2021-03-09 |
| Distributed | Nationwide (US) |
| Quantity | 65 devices |
| Reason classes | device malfunction |
| Model numbers | 9784220831 |
Product
Apollo DRF; Model: 9784220831 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
Reason for recall
Patient fell from the table because the footrest of the device detached from the table top while the patient was positioned on the table and table was moving from vertical position.
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-1429-2017. 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.