Kingfisher Compact Individual First Aid Kit Recall
Areazine synthesizes this FDA recall directly from FDA's official public data feed. See our methodology for full source attribution and refresh cadence.
Integrated Medcraft LLC is recalling Kingfisher Compact Individual First Aid Kits because the Guedel Airway components may be occluded or partially occluded.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 20, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, MedicalDevices.
What Happened
The recall was initiated because the devices could potentially contain an occluded or partially occluded Guedel Airway tip.
Which Products Are Affected
Kingfisher Compact Individual First Aid Kit, REF Number: 76656, Lot Numbers: IMC-00000132, IMC-00000139. The affected One-piece Guedel airway components are:
- Size 00, ISO 5.0, blue, Product Code: 1100050, Lot Numbers: 32121232, 32208193, 32400267, 32403734, 32408819, 32409672, 32416545, 32427064, 32605471, 32606405, 32606850, 32607154
- Size 000, ISO 3.5, light green, Product Code: 1000035, Lot Numbers: 32190425, 32213076, 32221283, 32307261, 32317627, 32321305, 32513841, 32517565 The recall affects US Nationwide distribution.
What You Should Do
Consumers should verify the lot numbers of their Kingfisher Compact Individual First Aid Kit against the affected lots listed in the recall.
Why This Matters
This Class II recall involves a medical device distributed nationwide that may pose a risk of temporary or reversible adverse health consequences.
Source
FDA recall number Z-2837-2026. Recalling firm: INTEGRATED MEDCRAFT LLC, East Hampton, CT.
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (1,140 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 20, 2026.
Frequently Asked Questions
Common questions about this FDA recall.