Stop using now Medical device recall · FDA · Published July 7, 2026

Medcraft Kingfisher First Aid Kit Recall: Risk of Airway Blockage

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2837-2026Medical device Medcraft ›

Stop using this now

Devices could potentially contain an occluded or partially occluded Guedel Airway tip.

✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/314274-medcraft-kingfisher-first-aid-kit-recall-risk-of-airway-blockage.

Source Summary by GovInfoNow · govinfonow.com/recall/314274-medcraft-kingfisher-first-aid-kit-recall-risk-of-airway-blockage · Updated August 18, 2026 · FDA enforcement record: FDA #Z-2837-2026

Cite this page

“Medcraft Kingfisher First Aid Kit Recall: Risk of Airway Blockage.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/314274-medcraft-kingfisher-first-aid-kit-recall-risk-of-airway-blockage. Based on FDA recall #Z-2837-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2837-2026%22&limit=1).

The FDA announced on July 7, 2026, that Integrated Medcraft LLC is recalling Kingfisher Compact Individual First Aid Kits containing potentially occluded Guedel airways. The agency issued recall number Z-2837-2026 for the Class II voluntary recall.

How to tell if you have it

Brand: Medcraft
Product: Kingfisher Compact Individual First Aid Kit, REF Number: 76656
Lot Numbers: IMC-00000132, IMC-00000139, 32121232, 32208193, 32400267, 32403734, 32408819, 32409672, 32416545, 32427064, 32605471, 32606405, 32606850, 32607154, 32190425, 32213076, 32221283, 32307261, 32317627, 32321305, 32513841, 32517565
Product Codes: 1100050 (Size 00, ISO 5.0, blue), 1000035 (Size 000, ISO 3.5, light green)
Distribution: US Nationwide

The hazard

According to the FDA, the devices could potentially contain an occluded or partially occluded Guedel Airway tip.

Context

GovInfoNow's records show Integrated Medcraft LLC has faced other recent recalls of similar products, including a Medline Airway Exam Kit Recall on Feb. 16, 2026, and a Medline Medical Kits Recall on March 24, 2026. Other recent recalls of similar products include a Medline 14 Fr Suction Catheter Kits Recall (Dec. 24, 2025).

How to tell if you have this one

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).

Brand
Medcraft
Category
Medical device

FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class II
Status
Ongoing
Distribution
US Nationwide distribution.

Recall number	Product, codes & lots	Quantity
Z-2836-2026	FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number: 1011-40002. 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.; FORWARD Oral Airway Kit (OPA Sizes 5, 6.5, 7, 8, 9, 10, 12). REF Number: 1011-40002. Lot Numbers: IMC-00000060, IMC-00000066, IMC-00000078, IMC-00000086, IMC-00000092, IMC-00000096, IMC-00000096, IMC-00000097, IMC-00000103, IMC-00000110, IMC-00000125, IMC-00000151, IMC-00000200, IMC-00000201, IMC-00000204, IMC-00000205. 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	509 units
Z-2837-2026	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.; 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	—

Based on the official FDA remedy

What to do — step by step

Stop using it now
Immediately stop using the recalled Kingfisher Compact First Aid Kits with potentially occluded airway tips.

Where it went and when

Where it was distributed

Distributed nationwide.

FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 36 days after the firm started it.

Jul 7, 2026Firm started the recall
Jul 31, 2026FDA classified it Class II
Aug 12, 2026Published in FDA’s Enforcement Report
Aug 18, 2026Added to GovInfoNow

Dates from the agency record only; steps without a date are left out.

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Link to this recall

<a href="https://govinfonow.com/recall/314274-medcraft-kingfisher-first-aid-kit-recall-risk-of-airway-blockage">Medcraft Kingfisher First Aid Kit Recall: Risk of Airway Blockage (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-2837-2026 (July 7, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2837-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.