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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K160764
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Recall
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FDA Recall
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Infant AirLife single-limb, continuous-flow circuit (Model AH132) containing AirLife Humidification ... 1 01/24/2018 Vyaire Medical
Adult AirLife dual-limb, dual-heat circuit (Model AH280) with AirLife Humidification Chamber, Model ... 1 01/24/2018 Vyaire Medical
Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification Chamber, Model Number A... 1 01/24/2018 Vyaire Medical
Infant AirLife Dual-,limb, dual-heat, high-flow circuit (Model AH265) with AirLife Humidification Ch... 1 01/24/2018 Vyaire Medical
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