Device recall
Z-0102-2023: ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr…
FDA device recall · Class II · ARROW INTERNATIONAL Inc.
Key facts
| Recall number (Z-number) | Z-0102-2023 |
|---|---|
| Recall event | 90871 |
| Product | ARROW Pressure Injectable Arrowg+ard Blue Advance Two-Lumen Midline Kit, 5.5 Fr, 15 cm, .018 Inch dia., REF ASK-41552-JHVA1. For peripheral access to the venous system for intravenous therapy, blood sampling, infusion, and pressure injection of contrast media. |
| Product code | PND |
| Recalling firm | ARROW INTERNATIONAL Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 19, 2024 |
| 510(k) numbers | K161313 |
| FEI number | 3013162291 |
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