Medical Device Recalls
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1 result found
510(K) Number: K162413 |
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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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V-PRO 60 Low Temperature Sterilization System (UDI: 00724995152000) | 2 | 02/13/2018 | Steris Corporation |
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