# FDA recall Z-1256-2023

> **Stryker Medical Division of Stryker Corporation** · Class II · device recall initiated 2023-02-01.

## Product

Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location.  Model: 650705550001

## Reason for recall

Transport Cot has insufficient volume of epoxy to assemblies installed in the head section and foot sectioning system may result in separation of head end or foot end from the cot and result in unexpected disengagement while loading/unloading or transport.

## Distribution

US Nationwide distribution in the states of NY, VA.

## Key facts

- **Recall number:** Z-1256-2023
- **Recalling firm:** Stryker Medical Division of Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-02-01
- **Report date:** 2023-03-22

- **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-1256-2023

## Citation

> AI Analytics. FDA recall Z-1256-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1256-2023. Source: US FDA. Licensed CC0.

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