Drug recall
King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in…
FDA recall event 66189 · Class II · King Systems Corp.
Key facts
| Event ID | 66189 |
|---|---|
| Recall numbers | Z-0002-2014 |
| Recalling firm | King Systems Corp. |
| Product type | Devices |
| Products | King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is intended for use in adult patients (in excess of 25 kg) for controlled ventilation during anesthesia for procedures that are short in… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | On December 13, 2012, King Systems initiated a voluntary recall of one (1) case(s) (5) individual products) from one (1) lot [(IV1V3) 62 cases, 310 products]of King LTSD Oropharyngeal Airways because… |
| Initiation date | Dec 13, 0012 |
| Report date | Oct 9, 2013 |
| Termination date | Nov 8, 2013 |
| City | Noblesville |
| State | IN |
| Country | United States |
| FEI number | 1824226 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: