Medical Device Recalls
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1 to 4 of 4 Results
PMA Number: P030047 |
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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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PRECISE PRO RX CAROTID STENT implant system, Product Codes: PC0520RXC, PC0530RXC, PC0540RXC, PC0620... | 1 | 03/15/2021 | Cordis Corporation |
Cordis Precise Nitinol Stent System. The Cordis PRECISE Nitinol Stent System devices are designe... | 2 | 12/20/2019 | Cardinal Health Inc. |
Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid) | 2 | 06/10/2016 | Cordis Corporation |
Cordis PRECISE (R) RX Nitinol Stent System (Biliary) | 2 | 06/10/2016 | Cordis Corporation |
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