Z-2837-2026 Class II Ongoing
FDA device recall Z-2837-2026 was initiated by INTEGRATED MEDCRAFT LLC on July 7, 2026 and is designated Class II. Reason for recall: Devices could potentially contain an occluded or partially occluded Guedel Airway tip. The recall status is ongoing.
Recall Details
- Product Type
- Devices
- Report Date
- August 12, 2026
- Initiation Date
- July 7, 2026
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
Product Description
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 for Recall
Devices could potentially contain an occluded or partially occluded Guedel Airway tip.
Distribution Pattern
US Nationwide distribution.
Code Information
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