Medical Device Recalls
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1 result found
510(K) Number: K190557 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic Bio-Medicus Insertion Kits, Model number 96553, Pediatric Insertion Kit, Sterile; and Mode... | 2 | 10/01/2021 | Medtronic Perfusion Systems |
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