Device recall
Z-0464-2023: Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label)…
FDA device recall · Class II · Medical Action Industries, Inc. 306
Key facts
| Recall number (Z-number) | Z-0464-2023 |
|---|---|
| Recall event | 91065 |
| Product | Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries Inc. IV Start Kit, REF #78019 (on kit label), sterile. Kit components are the Port Access Kit. |
| Product code | OWL |
| Recalling firm | Medical Action Industries, Inc. 306 |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 25, 2025 |
| FEI number | 1030451 |
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