Medical Device Recalls
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1 result found
510(K) Number: K024069 |
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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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| DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr) | 2 | 01/17/2025 |
FEI # 1000116158 Medtronic Perfusion Systems |
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