Class II — Oakworks Inc
| Recalling firm | Oakworks, INC. |
|---|---|
| Registered facility | OAKWORKS, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The warning label was printed with the incorrect weight capacity. The correct weight limit is 400 lbs., but the label states 500 lbs. |
| Product | Oakworks Bed (Emergency Field Bed); Model No. OBMPBR361980A6TTGRCS |
| Quantity | 109 |
| Distribution | US Nationwide distribution in the states of MA, NJ, and PA. |
| Initiated | 2022-04-21 |
| Classified | 2022-06-06 |
| Terminated | 2024-09-19 |
| Recall number | Z-1239-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Oakworks Inc (Z-1239-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90172/
Alerts for Oakworks, INC.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.