PX200 Emergency Relief Bed — Class II medical device recall Z-1238-2022
Terminated recall by Oakworks Inc, reported 2022-06-15, distributed nationwide. Product label was printed without the UDI number and warning label was printed with the incorrect weight capac
| Recall number | Z-1238-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Oakworks Inc, New Freedom, PA, United States |
| Recall initiated | 2022-04-21 |
| Classified | 2022-06-06 |
| Reported by FDA | 2022-06-15 |
| Terminated | 2024-09-19 |
| Distributed | Nationwide (US) |
| Quantity | 130 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00817463026399 |
| Serial numbers | PXR769629, PXR769630, PXR769631, PXR769632, PXR769633, PXR769634, PXR769635, PXR769636, PXR769637, PXR769638, PXR769639, PXR769640, PXR769641, PXR769642, PXR769643, PXR769644, PXR769645, PXR769646, PXR769647, PXR769648, PXR769649, PXR769650, PXR769651, PXR769652, PXR769653 and 105 more |
| Model numbers | PXEXEB362280A6TTZZH4C19 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1238-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.