# FDA recall Z-0479-2023

> **Stryker Medical Division of Stryker Corporation** · Class II · device recall initiated 2022-11-11.

## Product

Power-PRO 2, Model No. 6507, Item No. 650705550001 (US); 650700000000 (International)

## Reason for recall

Cot may experience unintended motion due to damaged cables. Potential risk of soft tissue injury to patients such as scrapes or bruises resulting from the cot lowering faster than expected.

## Distribution

Worldwide Distribution: US (Nationwide) and Foreign to countries of: Australia, Canada, Netherlands, and United Kingdom.

## Key facts

- **Recall number:** Z-0479-2023
- **Recalling firm:** Stryker Medical Division of Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-11-11
- **Report date:** 2022-12-21

- **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-0479-2023

## Citation

> AI Analytics. FDA recall Z-0479-2023. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-0479-2023. Source: US FDA. Licensed CC0.

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