[Recalled] 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 C
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| 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. |
|---|---|
| Brand / manufacturer | INTEGRATED MEDCRAFT LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2837-2026 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 07 July 2026 |
| EAN / barcode | 00000132 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
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This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.