Ultrasound EA — Class II medical device recall Z-0729-2024
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-0729-2024 |
|---|---|
| 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 | 20 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00817463025422 |
Product
Ultrasound EA (Ergonomic Advantage) table versions; G3 Multi-Specialty Echocardiography and Multi-Specialty with Electric Access Back Supports [left & right}
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-0729-2024. 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.