Device recall
Z-1869-2017: Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w…
FDA device recall · Class II · Elcam Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1869-2017 |
|---|---|
| Recall event | 76446 |
| Product | Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w gxl:w1/r rbls Product Usage: indicated for fluid flow directional control and for providing access ports for administration of intravenous solutions. Typical uses include pressure monitoring, intravenous fluid administration… |
| Product code | FMG |
| Recalling firm | Elcam Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 8, 2018 |
| 510(k) numbers | K060231 |
| FEI number | 3003649401 |
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