Medical Device Recalls
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1 result found
510(K) Number: K855144 |
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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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| TourniKwik Tourniquet Set (CFN 79012) | 2 | 07/23/2024 |
FEI # 1000116158 Medtronic Perfusion Systems |
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