Device recall
Z-2165-2013: Baxa Vial Adapter, 14mm - Luer Lock, Order No. REF: 90, Quantity: 50 each…
FDA device recall · Class II · Baxa Corporation
Key facts
| Recall number (Z-number) | Z-2165-2013 |
|---|---|
| Recall event | 66082 |
| Product | Baxa Vial Adapter, 14mm - Luer Lock, Order No. REF: 90, Quantity: 50 each, Single Use. Product Code H93890. Used as a needleless access device for reconstitution and drug transfer. |
| Product code | LHI |
| Recalling firm | Baxa Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 19, 2016 |
| 510(k) numbers | K900585 |
| FEI number | 1419106 |
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