INTEGRATED MEDCRAFT LLC recalls Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affe…

Devices could potentially contain an occluded or partially occluded Guedel Airway tip.

Firm initially notified customers on June 23, 2026 via email and June 24,2026 via postal mail. Updated letters were sent on July 7, 2026 via email. Customers were instructed to immediately discontinue use of affected product and inspect inventory for affected product. Customers should return affected product to Integrated MedCraft. If the customer has further distributed affected product, they should notify customers who received the product.

• FDA enforcement recordOfficial FDA database entry for Z-2837-2026
• FDA device classification · OHOOfficial FDA classification for this device type
• CFR regulation · 21 CFR 878.4014The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find INTEGRATED MEDCRAFT LLCSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.