Vascular Table without Fowler — Class II medical device recall Z-2349-2021
Terminated recall by Oakworks Inc, reported 2021-09-01, distributed nationwide. Weld failure- the bracket attaches the tabletop tilting actuator to the tabletop frame. If the bracket weld fa
| Recall number | Z-2349-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Oakworks Inc, New Freedom, PA, United States |
| Recall initiated | 2021-06-29 |
| Classified | 2021-08-25 |
| Reported by FDA | 2021-09-01 |
| Terminated | 2023-10-05 |
| Distributed | Nationwide (US) |
| Quantity | 55 units |
| Model numbers | 64219, 66783, USGNV22723723MTTZZCE2S, VCF766794 |
Product
Vascular Table without Fowler (USV1) and Ultrasound Vascular Table with Fowler (USV2). Intended Use: Vascular Ultrasound examination table Catalog Number: 66783 and 64219
Reason for recall
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
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-2349-2021. 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.