Device recall
Z-0283-2025: Brand Name: Vial2Bag Advanced Product Name: Vial2Bag Advanced 20mm Admixture…
FDA device recall · Class II · West Pharmaceutical Services AZ, Inc.
Key facts
| Recall number (Z-number) | Z-0283-2025 |
|---|---|
| Recall event | 95449 |
| Product | Brand Name: Vial2Bag Advanced Product Name: Vial2Bag Advanced 20mm Admixture Device Model/Catalog Number: 6070030 Software Version: Not applicable Product Description: The Vial2Bag Advanced 20mm Admixture Device is a single use, fluid transfer device that allows for the reconstitution and transfer… |
| Product code | LHI |
| Recalling firm | West Pharmaceutical Services AZ, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K201415 |
| FEI number | 3015176617 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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