Medical Device Recalls
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1 result found
510(K) Number: K173489 |
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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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Covidien HysteroLux Fluid Management System Control Unit, REF: 72205000 | 2 | 09/24/2021 | WOM World of Medicine AG |
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