Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K031383 |
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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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Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Cir... | 2 | 12/15/2015 | Teleflex Medical |
Hudson RCI, Breathing Circuit, Adult, Single Limb w/Heated Wire, [Respiratory Gas Humidifier, (Direc... | 2 | 07/23/2014 | Teleflex Medical |
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