Medical Device Recalls
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1 result found
510(K) Number: K153293 |
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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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Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034... | 2 | 04/29/2021 | B. Braun Medical, Inc. |
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