Ultrasound EA — Class II medical device recall Z-0727-2024
Ongoing recall by Oakworks Inc, reported 2024-01-24, distributed nationwide. Backrest platform stress fracture - the table is not operational in an inclined position
| Recall number | Z-0727-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Oakworks Inc, New Freedom, PA, United States |
| Recall initiated | 2023-12-05 |
| Classified | 2024-01-12 |
| Reported by FDA | 2024-01-24 |
| Distributed | Nationwide (US) |
| Quantity | 212 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00817463025323 |
| Serial numbers | USE799725, USE799726, USE799727, USE799730, USE799732, USE801427, USE801767, USE802125, USE802575, USE802576, USE803256, USE803299, USE803300, USE803589, USE803752, USE805081, USE805082, USE805279, USE805280, USE805281, USE805493, USE805494, USE805495, USE805794, USE805795 and 187 more |
Product
Ultrasound EA (Ergonomic Advantage) table versions; G2 (GENERAL 2) -An Ultrasound examination table
Reason for recall
Backrest platform stress fracture - the table is not operational in an inclined position
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-0727-2024. 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.