FDA recall Z-0918-2026

Stryker Medical Division of Stryker Corporation · Class II · device

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.

Distribution

US, nationwide

Key facts

Status
Ongoing
Initiation date
2025-10-31
Report date
2025-12-17
Voluntary/Mandated
Voluntary: Firm initiated
Location
Portage, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0918-2026