Device recall
Z-2089-2011: Argon Medical Devices, Arterial Line Kit, Arterial Catheter Mini Kit 20gax6in…
FDA device recall · Class II · Argon Medical Devices, Inc
Key facts
| Recall number (Z-number) | Z-2089-2011 |
|---|---|
| Recall event | 58289 |
| Product | Argon Medical Devices, Arterial Line Kit, Arterial Catheter Mini Kit 20gax6in, Part Number 498101, Lot 99767264 Multi-purpose Kit blister tray coupled with Tyvek lid stock heat-sealed to form a sterile barrier. |
| Product code | FTN |
| Recalling firm | Argon Medical Devices, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 24, 2012 |
| FEI number | 1625425 |
At a glance
- None Linked 510(k)s
- 10–99 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