Class II — INTEGRATED MEDCRAFT LLC
| Recalling firm | Integrated Medcraft LLC |
|---|---|
| Registered facility | INTEGRATED MEDCRAFT LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Devices could potentially contain an occluded or partially occluded Guedel Airway tip. |
| Product | 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. |
| Initiated | 2026-07-07 |
| Classified | 2026-07-31 |
| Recall number | Z-2837-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — INTEGRATED MEDCRAFT LLC (Z-2837-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99295/
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