Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K091626 |
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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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CryoPatch SG Pulmonary Hemi-Artery Patch | 2 | 04/25/2019 | CryoLife, Inc. |
CryoPatch SG Pulmonary Hemi-Artery, 1 graft | 2 | 10/18/2018 | CryoLife, Inc. |
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