Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K984053 |
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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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Medtronic REF 46915 Duet External Drainage and Monitoring system, Interlink Injection sites, Ventric... | 2 | 08/17/2023 | Medtronic Neurosurgery |
Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Catalog No. 46914... | 1 | 06/27/2014 | Medtronic Neurosurgery |
Medtronic Duet External Drainage and Monitoring System, SmartSite Injection Sites, Ventricular Cathe... | 1 | 06/27/2014 | Medtronic Neurosurgery |
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Lumbar Catheter, ... | 1 | 06/27/2014 | Medtronic Neurosurgery |
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Catalog No. 46913... | 1 | 06/27/2014 | Medtronic Neurosurgery |
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, Ventricular Cathe... | 1 | 06/27/2014 | Medtronic Neurosurgery |
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