Class II — Oakworks Inc
| Recalling firm | Oakworks, INC. |
|---|---|
| Registered facility | OAKWORKS, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Weld failure- the bracket attaches the tabletop tilting actuator to the tabletop frame. If the bracket weld fails, the tabletop tilting action is non-functional |
| Product | Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2). Intended Use: Vascular Ultrasound examination table Catalog Number: 66783 and 64219 |
| Quantity | 55 units |
| Distribution | Nationwide |
| Initiated | 2021-06-29 |
| Classified | 2021-08-25 |
| Terminated | 2023-10-05 |
| Recall number | Z-2349-2021 |
| 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-2349-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88365/
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.