Device recall
Z-2458-2015: Central Line >34 Weeks Kit. Cardiology department. The Central Line >34 Weeks…
FDA device recall · Class II · Medline Industries Inc
Key facts
| Recall number (Z-number) | Z-2458-2015 |
|---|---|
| Recall event | 71889 |
| Product | Central Line >34 Weeks Kit. Cardiology department. The Central Line >34 Weeks Kit (DYNDC1987A) is intended for use on patients greater than 34 weeks of age. The central venous catheter, also called a central line, is a long, thin, flexible tube used to give medicines, fluids, nutrients, or blood… |
| Product code | OFF |
| Recalling firm | Medline Industries Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 5, 2017 |
| FEI number | 1417592 |
At a glance
- None 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