Device recall
Z-1878-2011: King System, King LTSD Kit Size 4, non-sterile, REF KLTSD414, Manufacturer…
FDA device recall · Class II · King Systems Corp.
Key facts
| Recall number (Z-number) | Z-1878-2011 |
|---|---|
| Recall event | 57810 |
| Product | King System , King LTSD Kit Size 4, non-sterile, REF KLTSD414, Manufacturer: King Systems Noblesville, IN. Ventilation during anesthesia during procedures of short duration. An oropharyngeal airway is a device inserted through the mouth to provide a patent airway. |
| Product code | CAE |
| Recalling firm | King Systems Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 29, 2012 |
| FEI number | 1824226 |
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