# FDA recall Z-2349-2021

> **Oakworks Inc** · Class II · device recall initiated 2021-06-29.

## 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

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-2349-2021
- **Recalling firm:** Oakworks Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-06-29
- **Report date:** 2021-09-01
- **Termination date:** 2023-10-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New Freedom, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2349-2021

## Citation

> AI Analytics. FDA recall Z-2349-2021. Retrieved 2026-07-12 from https://api.ai-analytics.org/recall/Z-2349-2021. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*