Device recall
Z-0767-2019: Vial2BAG DC 13mm, REF 6070111, Single use only, Rx Only
FDA device recall · Class I · WEST PHARMA. SERVICES IL, LTD
Key facts
| Recall number (Z-number) | Z-0767-2019 |
|---|---|
| Recall event | 81877 |
| Product | Vial2BAG DC 13mm, REF 6070111, Single use only, Rx Only |
| Product code | LHI |
| Recalling firm | WEST PHARMA. SERVICES IL, LTD |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 20, 2022 |
| 510(k) numbers | K170095 |
| FEI number | 3000223297 |
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