Device recall
Z-0815-2009: King Systems 37" Universal Flex2 Extension Kit, 50 per case, King Systems…
FDA device recall · Class II · King Systems Corp.
Key facts
| Recall number (Z-number) | Z-0815-2009 |
|---|---|
| Recall event | 48991 |
| Product | King Systems 37" Universal Flex2 Extension Kit, 50 per case, King Systems Corporation, Noblesville, IN; REF # XF37. |
| Product code | CAI |
| Recalling firm | King Systems Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 12, 2009 |
| FEI number | 1824226 |
At a glance
- None Linked 510(k)s
- 100–999 Products in the same recall event
- 100–999 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