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INTEGRATED MEDCRAFT LLC: Kingfisher Compact Individual First Aid Kit. REF

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Devices could potentially contain an occluded or partially occluded Guedel Airway tip.. Recalled by INTEGRATED MEDCRAFT LLC. Distribution: US Nationwide distribution.. Classification (Class II — potential health risk). Affected lots/dates: Kingfisher Compact Individual First Aid Kit. REF Number: 76656. Lot Numbers: IMC-00000132, IMC-00000139. Containing the. Contact the manufacturer or the retailer where you purchased this device to arrange for a free correction, repair, or replacement.

Reward FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer
Category Product Recalls & Refunds
Location National
Eligibility U.S. consumers who own or purchased the recalled medical device. Contact the manufacturer or the retailer/pharmacy where you purchased it to arrange for a free correction, repair, or replacement. Have the model number ready if possible.
Source Official Source ↗
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