Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Containing the affected One-piece Guedel airway componen
FDA device recall Z-2837-2026 · posted 2026-07-31 · Open, Classified
Recall details
- Recalling firm
- INTEGRATED MEDCRAFT LLC
- Reason for recall
- Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
- Action taken
- 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.
- Root cause
- Component design/selection
- Status
- Open, Classified
- Product code
- OHO
- Distribution
- US Nationwide distribution.
- Date initiated
- 2026-07-07
- Date posted
- 2026-07-31
- Location
- East Hampton, CT
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