Device recall
Z-1754-2010: Xenon Diagnostic Circuit Kits labeled as "Xenon Diagnostic Circuit", "Xenon…
FDA device recall · Class II · Continental Medical Labs,Inc
Key facts
| Recall number (Z-number) | Z-1754-2010 |
|---|---|
| Recall event | 55527 |
| Product | Xenon Diagnostic Circuit Kits labeled as "Xenon Diagnostic Circuit", "Xenon Circuit", and Needleless Xenon Diagnostic Circuit" Manufactured for RAF MEDICAL, INC., (Model number's RAF2306, RAF2304, RAF2380, RAF2300, RAF2370, RAF2372, RAF2350, RAF2341, RAF2302, RAF2340 RAF2306, RAF2304, RAF2361), or… |
| Product code | CAH |
| Recalling firm | Continental Medical Labs,Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 5, 2012 |
| 510(k) numbers | K063526 |
| FEI number | 2128604 |
At a glance
- 1–9 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