Device recall
Z-1906-2016: Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve…
FDA device recall · Class II · B. Braun Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1906-2016 |
|---|---|
| Recall event | 73986 |
| Product | Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of medication from inverted bags or semi-rigid containers. Interavenous delivery of transferred medication(Device is not intended for direct infusion) |
| Product code | LHI |
| Recalling firm | B. Braun Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2017 |
| 510(k) numbers | K943181 |
| FEI number | 2523676 |
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