Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K101866 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CryoPatch SG Pulmonary Human Cardiac Patch. The patch is cryopreserved in a tissue culture medium c... | 2 | 12/21/2020 | CryoLife, Inc. |
| Cryopatch SG Pulmonary Human Cardiac Branch, Catalog Number SGP020 | 2 | 06/21/2018 | CryoLife, Inc. |
| Pulmonary Hemi-Artery SG Used in heart surgery | 2 | 01/23/2014 | CryoLife, Inc. |
| Pulmonary Hemi-Artery SG Used in heart surgery | 2 | 03/04/2011 | CryoLife, Inc. |
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