# FDA recall Z-0435-2024

> **Stryker Medical Division of Stryker Corporation** · Class II · device recall initiated 2023-08-30.

## Product

ProCurity bed series, model number 3009, item number: 3009PX-ZMX-600.

## Reason for recall

Patient beds are missing test values for electrical safety tests presenting risk of  tissue burn or electrical shock.

## Distribution

Distribution US Nationwide including Puerto Rico, Australia, Canada, Chile, China, Mexico, Poland, Spain and Switzerland.

## Key facts

- **Recall number:** Z-0435-2024
- **Recalling firm:** Stryker Medical Division of Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-30
- **Report date:** 2023-12-13

- **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-0435-2024

## Citation

> AI Analytics. FDA recall Z-0435-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0435-2024. Source: US FDA. Licensed CC0.

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