Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K160764 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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