Device recall
Z-0059-05: Arrowg+ard Blue Two Lumen CVC Super Kit, Catalog number AK-22802-SK. The kit…
FDA device recall · Class III · Arrow International Inc
Key facts
| Recall number (Z-number) | Z-0059-05 |
|---|---|
| Recall event | 30115 |
| Product | Arrowg+ard Blue Two Lumen CVC Super Kit, Catalog number AK-22802-SK. The kit actually contains Arrowg+ard Blue Plus Two Lumen CVC Super Kit. Catalog number AK-42802-SK, 8 Fr x 16 cm Two Lumen Arrowg+ard Blue Plus Catheters. The plus indicates that the line extension clamps are attached to the… |
| Product code | FOZ |
| Recalling firm | Arrow International Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Nov 30, 2004 |
| 510(k) numbers | K993691 |
| 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