# FDA recall Z-1239-2022

> **Oakworks Inc** · Class II · device recall initiated 2022-04-21.

## Product

Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCS

## Reason for recall

The warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label states 500 lbs.

## Distribution

US Nationwide distribution in the states of MA, NJ, and PA.

## Key facts

- **Recall number:** Z-1239-2022
- **Recalling firm:** Oakworks Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-04-21
- **Report date:** 2022-06-15
- **Termination date:** 2024-09-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New Freedom, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1239-2022

## Citation

> AI Analytics. FDA recall Z-1239-2022. Retrieved 2026-07-03 from https://api.ai-analytics.org/recall/Z-1239-2022. Source: US FDA. Licensed CC0.

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