Device recall
Z-0975-2007: SafeClinitubes, REF 942-892, D957P-70-100x1, contained in kits containing 250…
FDA device recall · Class II · Radiometer America Inc
Key facts
| Recall number (Z-number) | Z-0975-2007 |
|---|---|
| Recall event | 37526 |
| Product | SafeClinitubes, REF 942-892, D957P-70-100x1, contained in kits containing 250 SafeClinitubes, insert, mixing wires and end caps. Capillary samplers for drawing small amounts of blood for blood gas analysis. |
| Product code | GIO |
| Recalling firm | Radiometer America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 8, 2012 |
| FEI number | 1523456 |
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