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U.S. Department of Health and Human Services

Medical Device Recalls

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21 to 30 of 500 Results *
Recall Date to: 09/01/2015
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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KimVent* Closed Suction System for Adults, 14 F, DSE (Product Code 2210); KimVent* Closed Suction Sy... 2 08/31/2015 Halyard Health, Inc
KimVent* Wet Pak* Closed Suction System for Adults, 14 F, DSE, MDI (Product 8224); KimVent* Wet Pak*... 2 08/31/2015 Halyard Health, Inc
KimVent* Closed Suction System for Adults, 14 F, DSE, MDI (Product Code 22108); KimVent* Closed Suct... 2 08/31/2015 Halyard Health, Inc
KimVent* Closed Suction System for Adults, 14 F, DSE, DT (Product Code 22109) A tracheobronchial su... 2 08/31/2015 Halyard Health, Inc
NovaPlus Trach Care* Closed Suction System for Adults, Double Swivel Elbow, Directional Tip, 14F (Pr... 2 08/31/2015 Halyard Health, Inc
NovaPlus Trach Care* Closed Suction System for Adults, Double Swivel Elbow, 14F (Product Code 2V2210... 2 08/31/2015 Halyard Health, Inc
KimVent* Turbo-Cleaning Closed Suction System for Adults, 14 F, DSE (Product Code 227); KimVent* Tur... 2 08/31/2015 Halyard Health, Inc
KimVent* Closed Suction Systems for Adults, 14 F, Qwik Clip (Product Code 2273) A tracheobronchial ... 2 08/31/2015 Halyard Health, Inc
KimVent* Turbo-Cleaning Closed Suction System for Adults, 14 F, T-Piece (Product Code 22705); KimVen... 2 08/31/2015 Halyard Health, Inc
KimVent* Turbo-Cleaning Closed Suction System for Adults, 14 F, DSE, MDI (Product Code 2271418) A t... 2 08/31/2015 Halyard Health, Inc

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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