FDA Device recall Z-2255-2013
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…
- FDA Device
- Class III
- terminated
- Published 2013-09-25
On 2013-09-25 the FDA classified a Class III recall of 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… by King Systems, citing report that size 5 KLTD airways were packaged in pouches indicating a size of 2.5 and shipped to your facility. The correct size of the KLTD airway is clearly marked on the actual….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2255-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-09-03 |
| Published | 2013-09-25 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | King Systems |
| Distribution | NY |
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.
Reason
Report that size 5 KLTD airways were packaged in pouches indicating a size of 2.5 and shipped to your facility. The correct size of the KLTD airway is clearly marked on the actual airway product and the physical size difference between 2.5 and 5 is distinct and obvious.
Identifiers
| code_info | Part Number KLTD2125 Lot Number I10RG |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2255-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.