Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K031666 |
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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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Arthrex Deltoid Ligament Reconstruction Implant System. Intended as a fixation post, a distributi... | 2 | 04/08/2016 | Arthrex, Inc. |
Datascope CS 100 Intra-Aortic Balloon Pump and Datascope CS 300 Intra-Aortic Balloon Pump, Datascop... | 2 | 01/31/2008 | Datascope Corp |
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