Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K200456 |
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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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| Becker External Drainage and Monitoring System: 24146 EDMS 24146 BECKER NO Y-SITE 25120 EDMS II 25... | 1 | 12/19/2024 | Medtronic Neurosurgery |
| Exacta External Drainage and Monitoring System: 27581 KIT 27581 EXACTA W/EDM VCATH 35CM 27636 EDM ... | 1 | 12/19/2024 | Medtronic Neurosurgery |
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