Sonesta S2 — Class II medical device recall Z-1894-2017
Terminated recall by Sonesta Medical Ab, reported 2017-05-10. The user / service manual for the Sonesta S2 Chair contain wrong information concerning the maximum patient we
| Recall number | Z-1894-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sonesta Medical Ab, Bromma, Sweden |
| Recall initiated | 2017-03-08 |
| Classified | 2017-04-28 |
| Reported by FDA | 2017-05-10 |
| Terminated | 2019-08-20 |
| Countries outside the US | CA, IT, LB, NL, TW |
| Quantity | 28 devices |
Product
Sonesta S2; Article numbers: 525-S2-110V and 525¿¿S2-220V
Reason for recall
The user / service manual for the Sonesta S2 Chair contain wrong information concerning the maximum patient weight.
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-1894-2017. 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.