Class II — Sonesta Medical Ab
| Recalling firm | Sonesta Medical AB |
|---|---|
| Registered facility | SONESTA MEDICAL AB (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The user / service manual for the Sonesta S2 Chair contain wrong information concerning the maximum patient weight. |
| Product | Sonesta S2; Article numbers: 525-S2-110V and 525®S2-220V |
| Quantity | 28 devices |
| Distribution | Worldwide Distribution - US Distribution to the state of : MA., and to the countries of : Canada, Netherlands, Dubai, Taiwan, Lebanon, Italy |
| Initiated | 2017-03-08 |
| Classified | 2017-04-28 |
| Terminated | 2019-08-20 |
| Recall number | Z-1894-2017 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Sonesta Medical Ab (Z-1894-2017).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/77075/
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