FDA Device recall Z-1894-2017
Sonesta S2
- FDA Device
- Class II
- terminated
- Published 2017-05-10
On 2017-05-10 the FDA classified a Class II recall of Sonesta S2 by Sonesta Medical Ab, citing the user / service manual for the Sonesta S2 Chair contain wrong information concerning the maximum patient weight.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1894-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-03-08 |
| Published | 2017-05-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Sonesta Medical Ab |
| Distribution | MA |
Product
Sonesta S2; Article numbers: 525-S2-110V and 525¿¿S2-220V
Reason
The user / service manual for the Sonesta S2 Chair contain wrong information concerning the maximum patient weight.
Identifiers
| code_info | 12-00001-110V 12-00011-110V 23-00002-220V (Demo Product) 12-00002-110V 12-00012-110V 23-00001-220V 12-00003-110V 12-000…12-00001-110V 12-00011-110V 23-00002-220V (Demo Product) 12-00002-110V 12-00012-110V 23-00001-220V 12-00003-110V 12-00013-110V 23-00003-220V 12-00004- 110V 12-00014-110V 23-00004-220V 12-00005-110V 12-00015-110V 23-00005-220V 12-00006-110V 12-20001-110V 23-00006-220V 12-00007-110V 12-20002-110V 23-00009-220V 12-00008-110V 12-20003-110V 23-00020-220V 12-00009-110V 12-20004 -110V 23-20001-220V 12-00010-110V 23-20002-220V |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1894-2017%22
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