- Recalling firm
- INTEGRATED MEDCRAFT LLC
- Reason for recall
- Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
- Affected products (lot / model / serial)
- Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Lot Numbers: IMC-00000132, IMC-00000139. Containing the affected One-piece Guedel airway components 1. Size 00, ISO 5.0, blue. Product Code: 1100050. Lot Numbers: 32121232, 32208193, 32400267, 32403734, 32408819, 32409672, 32416545, 32427064, 32605471, 32606405, 32606850, 32607154. 2. Size 000, ISO 3.5, light green. Product Code: 1000035. Lot Numbers: 32190425, 32213076, 32221283, 32307261, 32317627, 32321305, 32513841, 32517565
- Distribution pattern
- US Nationwide distribution.
- Firm location
- East Hampton, CT, United States
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-2837-2026
- Recall initiated
- July 7, 2026
- FDA classification date
- July 31, 2026
- FDA report date
- August 12, 2026
- FDA event ID
- 99295
- Last updated on HTM Vibe
- August 18, 2026