Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K991653 |
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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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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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