Stryker MV3 bariatric bed — Class II medical device recall Z-0918-2026
Ongoing recall by Stryker Medical Division of Stryker Corporation, reported 2025-12-17, distributed nationwide. Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these pr
| Recall number | Z-0918-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Medical Division of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2025-10-31 |
| Classified | 2025-12-11 |
| Reported by FDA | 2025-12-17 |
| Distributed | Nationwide (US) |
| Quantity | 294 units |
| UPC / GTIN / UDI-DI | 02020013200103, 02021013200087, 02021013200247, 02021013200278, 02021013200353, 02022013200107, 02022013200114, 02022013200145, 02023013200005, 02023013200036, 02023013200098, 02023013200128, 02023013200135, 02023013200159, 02023013200166, 02024013200019, 02024013200057, 02024013200064, 02024013200095, 02024013200125, 02024013200156, 02024013200187, 02024013200248, 02024013200255, 02024013200286 and 6 more |
| Serial numbers | 2020013200012, 2020013200103, 2020013200114, 2020013200115, 2020013200136, 2020013200137, 2021013200017, 2021013200021, 2021013200038, 2021013200039, 2021013200040, 2021013200079, 2021013200080, 2021013200087, 2021013200089, 2021013200091, 2021013200092, 2021013200093, 2021013200096, 2021013200098, 2021013200099, 2021013200102, 2021013200114, 2021013200122, 2021013200133 and 269 more |
| Model numbers | 5900000001 |
Product
Stryker MV3 bariatric bed, Part Number 5900000001
Reason for recall
Stryker has issued a voluntary recall of certain MV3 beds and Arise 1000EX mattresses because some of these products have been sold in close proximity, suggesting a potential intent for them to be used together. These products have not been tested for compatibility and thus are not designed to be used together. The combination of both is not recommended by Stryker.
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-0918-2026. 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.