Device recall
Z-2072-2020: Kiwi Complete Vacuum Delivery System, Model No. VAC-6000MTE - Product Usage: The…
FDA device recall · Class II · Clinical Innovations, LLC
Key facts
| Recall number (Z-number) | Z-2072-2020 |
|---|---|
| Recall event | 85170 |
| Product | Kiwi Complete Vacuum Delivery System, Model No. VAC-6000MTE - Product Usage: The Kiwi is a disposable vacuum-assisted fetal delivery system. |
| Product code | HDB |
| Recalling firm | Clinical Innovations, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 16, 2022 |
| 510(k) numbers | K981260 |
| FEI number | 1000220650 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database