Device recall
Z-0985-2011: KING LT -D Lanyngeal Tube, Size 3, KLTD203, King Systems Corporation 15011…
FDA device recall · Class II · King Systems Corp.
Key facts
| Recall number (Z-number) | Z-0985-2011 |
|---|---|
| Recall event | 54350 |
| Product | KING LT -D Lanyngeal Tube, Size 3, KLTD203, King Systems Corporation 15011 Herriman Boulevard, Noblesville, IN 46060. Intended use: Airway management by providing a patent airway to allow patient ventilation. |
| Product code | CAE |
| Recalling firm | King Systems Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 16, 2012 |
| 510(k) numbers | K021634, K033186 |
| FEI number | 1824226 |
At a glance
- 1–9 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