Device recall
Z-2255-2013: King LT-D Oropharyngeal Airways The King LT-D is intended for use in adult…
FDA device recall · Class III · King Systems Corp.
Key facts
| Recall number (Z-number) | Z-2255-2013 |
|---|---|
| Recall event | 66185 |
| Product | King LT-D Oropharyngeal Airways The King LT-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in duration and when the patient is considered to have a low risk of aspiration of stomach contents. |
| Product code | CAE |
| Recalling firm | King Systems Corp. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 15, 2014 |
| 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