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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: K915226
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FDA Recall
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AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector; an Rx device for single... 1 06/29/2012 FEI # 3008002452
Carefusion 2200 Inc
AirLife Isothermal Breathing Circuit, Infant Respiratory Circuit, Heated; an Rx device for single pa... 1 06/29/2012 FEI # 3008002452
Carefusion 2200 Inc
AirLife Isothermal Breathing Circuit, Infant Respiratory Circuit, Non-Heated; an Rx device for singl... 1 06/29/2012 FEI # 3008002452
Carefusion 2200 Inc
CareFusion AirLife Heated Infant Breathing Circuit Product Usage: Respiratory breathing circuits... 2 09/23/2014 FEI # 3008002452
Carefusion 2200 Inc
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