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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: K991653
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Product Description
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Recall
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FDA Recall
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InVision-Plus and InVision-Plus Junior Needleless IV Connector, Disposable, Single Use Products a... 2 01/21/2016 Rymed Technologies, LLC
RYM-5001 InVision-Plus® Neutral Displacement I.V. Connector, packaged 100 units per box, 5 boxes per... 2 12/30/2006 Rymed Technologies, Inc.
RYM-5000 InVision-Plus® Neutral Displacement I.V. Connector, packaged 200 units per box, 5 boxes per... 2 12/30/2006 Rymed Technologies, Inc.
RYM-5000 InVision-Plus® NEUTRAL® I.V. Connector, packaged 200 units per box, 5 boxes per case (1000 ... 2 12/30/2006 Rymed Technologies, Inc.
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