Data Foundry

Medical device recalls 2025

Stryker Arise 1000EX mattress — Class II medical device recall Z-0919-2026

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 numberZ-0919-2026
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmStryker Medical Division of Stryker Corporation, Portage, MI, United States
Recall initiated2025-10-31
Classified2025-12-11
Reported by FDA2025-12-17
DistributedNationwide (US)
Quantity297 units
UPC / GTIN / UDI-DI00857268006608
Serial numbers1000007185, 1000007187, 1000007188, 1000007189, 1000046411, 1000046735, 1000048762, 1000053839, 1000055394, 1000065720, 1000066888, 1000160222, 1000181244, 1000183920, 1000183921, 1000184053, 1000213521, 1000213522, 1000213529, 1000213530, 1000213531, 1000213532, 1000213533, 1000214321, 1000214331 and 272 more
Model numbers2236000000

Product

Stryker Arise 1000EX mattress, Part Number 2236000000

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-0919-2026. 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.