Device recall
Z-1830-2012: Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R)…
FDA device recall · Class I · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-1830-2012 |
|---|---|
| Recall event | 61915 |
| Product | Arrow Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) ARROWgard Blue(R) Catheter Product Usage: The multiple-lumen catheter permits venous access to central circulation. |
| Product code | FOZ |
| Recalling firm | Arrow International Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 22, 2013 |
| 510(k) numbers | K900263 |
| 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