FDA Recall Terminated

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 duration and when the patient is considered to have a low risk of aspiration of stomach contents.

Recall: Z-0002-2014 · Initiated December 13, 0012

Recall

Recall Number
Z-0002-2014
Event Number
66189
Firm
King Systems Corp.
FEI Number
1824226
Product Code
CAE
Status
Terminated
Root Cause
Error in labeling
Initiated
December 13, 0012
Posted
October 1, 2013
Terminated
November 8, 2013
Address
15011 Herriman Blvd, Noblesville, IN, 46060-4253

Description

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 duration and when the patient is considered to have a low risk of aspiration of stomach contents.

Reason

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 the package label indicated that the airway was a size 5 when in fact the airway in the package was a size 4. When King manufacturers a lot, all of the components are the same size, part number etc. I

Action

King Systems notified the only one (1) consignee who received the affected product of the problem via a customer complaint. Five (5) of the five (5) affected products were destroyed by consignee.

Distribution

USA Nationwide Distribution in the state of NY

Quantity

1 case; 5 units