RecallRadar

FDA Device recall Z-2837-2026

Kingfisher Compact Individual First Aid Kit

On 2026-08-12 the FDA classified a Class II recall of Kingfisher Compact Individual First Aid Kit by Integrated Medcraft, citing devices could potentially contain an occluded or partially occluded Guedel Airway tip.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2837-2026
ClassificationClass II
Statusongoing
Initiated2026-07-07
Published2026-08-12
Last updated2026-09-13 11:58 UTC
CompanyIntegrated Medcraft
DistributionUS

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.

Identifiers

code_info
Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Lot Numbers: IMC-00000132, IMC-00000139. Containing th…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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2837-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.