Class II

Medical Device Recall: Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050. 2. Size 000, IS

INTEGRATED MEDCRAFT LLC · July 7, 2026

Reason for Recall

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

Product Description

Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050. 2. Size 000, ISO 3.5, light green. Product Code: 1000035.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2837-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

INTEGRATED MEDCRAFT LLC Medical Device Recall: Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway components: 1. Size 00, ISO 5.0, blue. Product Code: 1100050. 2. Size 000, IS | SafeCheck