First Aid Kit Recall: Integrated Medcraft Kingfisher Compact
Announced 2026-08-12 · FDA
FDA recalls the Kingfisher Compact Individual First Aid Kit (REF 76656) from Integrated Medcraft LLC due to potential occluded Guedel airway tips. The affected components are one-piece Guedel airways in sizes 00 (blue) and 000 (light green) with multiple listed lot numbers. The recall covers nationwide US distribution and no corrective action is listed.
| Brand | INTEGRATED MEDCRAFT LLC |
|---|---|
| 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. |
| Reason | Devices could potentially contain an occluded or partially occluded Guedel Airway tip. |
| Severity | moderate |
| Distribution | US Nationwide distribution. |
| Agency | FDA |
| Recall / campaign no. | 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 |
WHAT YOU SHOULD DO
- Do not use the affected kit.
- Contact Integrated Medcraft LLC for return, replacement, or disposal guidance and provide REF 76656 and the lot numbers.
- If you have used any affected components, consult a clinician and monitor for any airway-related issues.
Other INTEGRATED MEDCRAFT LLC recalls
This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.