Device recall
Z-2152-2008: Vitrex Blood Gas Capillary Tubes, MC0024, REF 189301, 250 pcs, 1,45 x 1,85 x 125…
FDA device recall · Class II · Opti Medical Systems Inc
Key facts
| Recall number (Z-number) | Z-2152-2008 |
|---|---|
| Recall event | 48435 |
| Product | Vitrex Blood Gas Capillary Tubes, MC0024, REF 189301, 250 pcs, 1,45 x 1,85 x 125 mm app. 200l, Heparinized: 6 IU Na & 9 IU Li/100 l, |
| Product code | GIO |
| Recalling firm | Opti Medical Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 22, 2010 |
| FEI number | 3004102403 |
At a glance
- None Linked 510(k)s
- 1–9 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