Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K202124 |
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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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PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU | 2 | 09/27/2021 | Aesculap Implant Systems LLC |
PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13 | 2 | 09/27/2021 | Aesculap Implant Systems LLC |
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