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Recall Observatory FDA recall evidence

Device product

KING LTSD,SIZE 1,W/SUCTION PORT STERILE-Inserted into a patient s pharynx through the mouth to provide patent airway. Model/Catalog Number: KLTSD421

Z-0270-2025

September 26, 2024

Class II

Product summary

Firm
King Systems Corp. dba Ambu, Inc.
Event
Event 95451
Status
Ongoing
Classification
Class II
Quantity
21939 units
Official record key
device-enforcement:Z-0270-2025

Official wording

Reason: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it introduces a new indication for pediatric use in an Oropharyngeal Airway.

Code information: UDI-DI: 00612649210162 (Shipper Label); 00612649210155 (Piece Label)

Distribution pattern: Nationwide

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because it introduces a new indication for pediatric use in an Oropharyngeal Airway.