Medcraft recalls Kingfisher Compact First Aid Kits with potentially occluded Guedel airway tips. Affected kits may cause breathing difficulties during emergencies. Stop using immediately if you own the recalled models.
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
Medcraft is recalling Kingfisher Compact First Aid Kits that may have a blocked airway tip. This could prevent proper breathing during emergencies, making the kits unsafe for use.
The airway tip in these kits could become partially or completely blocked, preventing air from flowing through during critical medical situations. This could lead to breathing difficulties or life-threatening complications if needed.
Anyone who owns the recalled Kingfisher Compact First Aid Kits. People using these kits during medical emergencies are at highest risk.
Check for the Kingfisher Compact First Aid Kit with REF Number 76656. Look for specific sizes: blue Size 00 (Product Code 1100050) or light green Size 000 (Product Code 1000035).
Immediately stop using the recalled Kingfisher Compact First Aid Kits with potentially occluded airway tips.
The airway tip could be partially or completely blocked, preventing proper airflow during emergencies.
Check for the Kingfisher Compact First Aid Kit with REF Number 76656. Look for specific sizes: blue Size 00 (Product Code 1100050) or light green Size 000 (Product Code 1000035).
Stop using it immediately. The recall does not provide a replacement or repair option.
We’ve drafted a message you can send Medcraft to request your refund or repair — edit it as you like.
Subject: Recall Z-2837-2026 — Medcraft Medcraft Hello, I own a Medcraft that is covered by recall Z-2837-2026 from Medcraft. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
