# FDA recall Z-0919-2026

> **Stryker Medical Division of Stryker Corporation** · Class II · device recall initiated 2025-10-31.

## 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.

## Distribution

US, nationwide

## Key facts

- **Recall number:** Z-0919-2026
- **Recalling firm:** Stryker Medical Division of Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-10-31
- **Report date:** 2025-12-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Portage, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0919-2026

## Citation

> AI Analytics. FDA recall Z-0919-2026. Retrieved 2026-09-08 from https://api.ai-analytics.org/recall/Z-0919-2026. Source: US FDA. Licensed CC0.

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