Device recall
Z-0051-2012: Outlook ES pump is intended for use with B. Braun Medical Inc. Horizon Pump IV…
FDA device recall · Class I · B Braun Medical, Inc
Key facts
| Recall number (Z-number) | Z-0051-2012 |
|---|---|
| Recall event | 59848 |
| Product | Outlook ES pump is intended for use with B. Braun Medical Inc. Horizon Pump IV Sets. Used to regulate the flow of primary and secondary fluids when positive pressure is required. The infusion system is capable of delivering fluid from a negative head height (when the IV fluid container is lower than… |
| Product code | FRN |
| Recalling firm | B Braun Medical, Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | May 4, 2015 |
| 510(k) numbers | K011975, K994375 |
| FEI number | 1641965 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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