Device recall
Z-2749-2015: Elcam Medical MANI 3G Plate BLS RAD B.BRAUN; Manifold for pressure monitoring…
FDA device recall · Class II · Elcam Medical, Inc.
Key facts
| Recall number (Z-number) | Z-2749-2015 |
|---|---|
| Recall event | 71880 |
| Product | Elcam Medical MANI 3G Plate BLS RAD B.BRAUN; Manifold for pressure monitoring and intravenous fluid administration. Manufactured by: Elcam Medical ACAL, Israel; Distributed by: Elcam Medical Inc., USA. Sterile |
| Product code | LZG |
| Recalling firm | Elcam Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 18, 2017 |
| 510(k) numbers | K122953 |
| 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