Device recall
Z-1672-2009: 12 French 3 Lumen 20 cm Large-Bore Central Venous Catheters. Product numbers…
FDA device recall · Class II · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-1672-2009 |
|---|---|
| Recall event | 52376 |
| Product | 12 French 3 Lumen 20 cm Large-Bore Central Venous Catheters. Product numbers AK-15123-H, AK-15123-J, CS-15123-E, and MC-15123. The large-bore multiple-lumen catheter permits venous access to the central circulation for rapid fluid administration. It may be inserted into the jugular, subclavian, or… |
| Product code | FOZ |
| Recalling firm | Arrow International Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 29, 2010 |
| 510(k) numbers | K970864 |
| FEI number | 3015859709 |
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