# FDA recall Z-2072-2020

> **Clinical Innovations, LLC** · Class II · device recall initiated 2019-08-06.

## Product

Kiwi Complete Vacuum Delivery System, Model No. VAC-6000MTE - Product Usage: The Kiwi is a disposable vacuum-assisted fetal delivery system.

## Reason for recall

There is a potential for loss of vacuum or failure to generate vacuum when using the firm's fetal vacuum delivery system.

## Distribution

OUS customers only.

## Key facts

- **Recall number:** Z-2072-2020
- **Recalling firm:** Clinical Innovations, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-08-06
- **Report date:** 2020-05-27
- **Termination date:** 2022-09-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Murray, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2072-2020

## Citation

> AI Analytics. FDA recall Z-2072-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2072-2020. Source: US FDA. Licensed CC0.

---

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