Kiwi Complete Vacuum Delivery System — Class II medical device recall Z-2072-2020
Terminated recall by Clinical Innovations, LLC, reported 2020-05-27. There is a potential for loss of vacuum or failure to generate vacuum when using the firm's fetal vacuum deliv
| Recall number | Z-2072-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Clinical Innovations, LLC, Murray, UT, United States |
| Recall initiated | 2019-08-06 |
| Classified | 2020-05-21 |
| Reported by FDA | 2020-05-27 |
| Terminated | 2022-09-16 |
| Quantity | 2,340 units |
| UPC / GTIN / UDI-DI | 00814247020659 |
| Lot numbers | 181144 |
| Model numbers | VAC-6000MTE |
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.
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-2072-2020. 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.