Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
King LT-D Oropharyngeal Airways The King LT-D is intended for Recalled by King Systems Corp. Due to Report that size 5 KLTD airways were packaged...
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 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.
Quantity: 9 cases; 45 products
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed to 1 state: NY
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