Device recall
Z-2574-2021: NAMIC Manifolds. (1) NAMIC Angiographic MANIFOLD, Medium Pressure, REF 64038301…
FDA device recall · Class II · Medline Industries Inc
Key facts
| Recall number (Z-number) | Z-2574-2021 |
|---|---|
| Recall event | 88516 |
| Product | NAMIC Manifolds. (1) NAMIC Angiographic MANIFOLD, Medium Pressure, REF 64038301, UPN H965640383011, 3 Valve Manifold, Off Star Handles, Ports on Right, Rx only, Sterile; (2) NAMIC Angiographic MANIFOLD, Medium Pressure, REF 64038303, UPN H965640383031, 3 Valve Manifold, On Star Handles, Ports on… |
| Product code | DTL |
| Recalling firm | Medline Industries Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 25, 2025 |
| 510(k) numbers | K782095 |
| FEI number | 1417592 |
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