CLASS II ONGOING Device recall · Reported 12 Aug 2026 · FDA Enforcement Report

Kingfisher Compact Individual First Aid Kit recalled

Integrated Medcraft is recalling Kingfisher Compact Individual First Aid Kit, distributed nationwide in the US. The recall was initiated on 7 Jul 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesKingfisher 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

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-2837-2026
FDA event ID: 99295
Recalling firm: Integrated Medcraft, East Hampton, CT
Classification: Class II
Status: Ongoing
Recall initiated: 7 Jul 2026
FDA classified: 31 Jul 2026
Reported: 12 Aug 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

7 Jul 2026	Recall initiated by company
31 Jul 2026	Classified by FDA	+24 days
12 Aug 2026	Published in enforcement report	+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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.

Where it was distributed

US Nationwide distribution.

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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

Where was it sold?

US Nationwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 99295

This product is part of a recall event; the main page for the event is Forward Oral Airway Kit (OPA Sizes 5, 6.5, 7 recalled.

Reported	Class	Recall	Company	Reason	Where
12 Aug 2026	CLASS II	Forward Oral Airway Kit (OPA Sizes 5, 6.5, 7 recalled	Integrated Medcraft	Other	Nationwide

More recalls from Integrated Medcraft

All 2

Reported	Class	Recall	Company	Reason	Where
12 Aug 2026Device	CLASS II	Forward Oral Airway Kit (OPA Sizes 5, 6.5, 7 recalled	Integrated Medcraft	Other	Nationwide

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