S3 MedSurg Bed — Class II medical device recall Z-2353-2016
Terminated recall by Stryker Medical Division of Stryker Corporation, reported 2016-08-17, distributed nationwide. CPU board failures cause fowler (backrest) electronic controls to stop working.
| Recall number | Z-2353-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Medical Division of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2016-02-02 |
| Classified | 2016-08-08 |
| Reported by FDA | 2016-08-17 |
| Terminated | 2017-06-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, MX |
| Quantity | 8,490 |
| Serial numbers | 141115067, 141115068, 141115069, 141115070, 141115071, 141115072, 141115073, 141115074, 141115075, 141115076, 141115077, 141115078, 141115079, 141115080, 141115081, 141115082, 141115083, 141115084, 141115085, 141115086, 141115087, 141115088, 141115089, 141115090, 141115091 and 475 more |
| Model numbers | 3005 |
Product
S3 MedSurg Bed, Model 3005. Stryker Medical
Reason for recall
CPU board failures cause fowler (backrest) electronic controls to stop working.
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-2353-2016. 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.