Device recall
Z-1322-06: Capillary (end) caps, accessory for use with blood gas analyzers included in…
FDA device recall · Class II · Radiometer America Inc
Key facts
| Recall number (Z-number) | Z-1322-06 |
|---|---|
| Recall event | 35775 |
| Product | Capillary (end) caps, accessory for use with blood gas analyzers included in Radiometer''s CLINITUBES kits. The end caps are packaged in bags. These bags are placed in the capillary tube kit which also contains: capillary tubes, end caps, mixing wires, and a magnet. Each kit may contain 1 or 5 bags… |
| Product code | GIO |
| Recalling firm | Radiometer America Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 24, 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