Cios Select VA 21 with FD- A Mobile X-ray system intended for use in… — Class II medical device recall Z-2240-2023
Ongoing recall by Siemens Medical Solutions USA, Inc, reported 2023-08-02, distributed nationwide. Incorrect glue was applied on the plexiglass sheet on the single tank cover assembly could potentially fall of
| Recall number | Z-2240-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Siemens Medical Solutions USA, Inc, Malvern, PA, United States |
| Recall initiated | 2023-06-05 |
| Classified | 2023-07-27 |
| Reported by FDA | 2023-08-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, BD, BR, CA, CH, CN, DE, ES, FR, GB, HR, ID, IT, JO, JP, LB, LU, MX, PE, PH, PL, RO, SK, SV, TW, UA, ZA |
| Quantity | 9 units |
| UPC / GTIN / UDI-DI | 04056869148243 |
Product
Cios Select VA 21 with FD- A Mobile X-ray system intended for use in Operating room, Traumatology, Endoscopy, Intensive Care Station, Pediatrics, Ambulatory patient care and in Veterinary Medicine. Material #11515088
Reason for recall
Incorrect glue was applied on the plexiglass sheet on the single tank cover assembly could potentially fall off and the ingress of liquid may occur, the risk of electric shock exists (e.g., ingress of a large amount of liquid following the plexiglass dropping off, at the same time the user or operator happens to touch the liquid on the cover which is connected to the internal live parts).
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-2240-2023. 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.