Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
King LTS-D Oropharyngeal Airways Product Usage: The King LTS-D is Recalled by King Systems Corp. Due to On December 13, 2012, King Systems initiated a...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact King Systems Corp. directly.
Affected 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 duration and when the patient is considered to have a low risk of aspiration of stomach contents.
Quantity: 1 case; 5 units
Why Was This Recalled?
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
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About King Systems Corp.
King Systems Corp. has 15 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report