# FDA recall Z-1238-2022

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

## Product

PX200 Emergency Relief Bed; Model No. PXEXEB362280A6TTZZH4C19

## Reason for recall

Product label was printed without the UDI number and 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-1238-2022
- **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-1238-2022

## Citation

> AI Analytics. FDA recall Z-1238-2022. Retrieved 2026-07-03 from https://api.ai-analytics.org/recall/Z-1238-2022. Source: US FDA. Licensed CC0.

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