Device recall
Z-0103-2013: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit, Pulset, 3 cc…
FDA device recall · Class II · Westmed Inc
Key facts
| Recall number (Z-number) | Z-0103-2013 |
|---|---|
| Recall event | 63276 |
| Product | Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit, Pulset, 3 cc, w/Crickett 23g x 1" A Needle, Luer Slip Barrel, 25U Balanced Heparin, No B Needle or Q-Cork, part number: 3363-95S. An arterial blood sampling kit is a device, in kit form, used to obtain arterial blood samples from a patient… |
| Product code | CBT |
| Recalling firm | Westmed Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 22, 2012 |
| FEI number | 1000374126 |
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