Class II — Oakworks Inc
| Recalling firm | Oakworks, INC. |
|---|---|
| Registered facility | OAKWORKS, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Backrest platform stress fracture - the table is not operational in an inclined position |
| Product | Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound examination table |
| Quantity | 212 units |
| Distribution | US Nationwide Distribution |
| Initiated | 2023-12-05 |
| Classified | 2024-01-12 |
| Recall number | Z-0727-2024 |
| 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-0727-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93595/
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