Device recall
Z-0418-2013: KING LAD SILI CONE SINGLE USE, King Systems devices/case, ETO Sterile. Size 2 /…
FDA device recall · Class II · King Systems Corp.
Key facts
| Recall number (Z-number) | Z-0418-2013 |
|---|---|
| Recall event | 63580 |
| Product | KING LAD SILI CONE SINGLE USE, King Systems devices/case, ETO Sterile. Size 2 / Infant Silicone King LAD Patient Size: 10-20kg Product Usage: Laryngeal airway |
| Product code | CAE |
| Recalling firm | King Systems Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 28, 2013 |
| FEI number | 1824226 |
At a glance
- None Linked 510(k)s
- 10–99 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