Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K810820 |
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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 I.M.A. Cannulae: DLP® 1 mm Arteriotomy Cannula, Model Number 31001 | 2 | 05/10/2024 | Medtronic Perfusion Systems |
Medtronic Vessel Cannulae: a) DLP® 2 mm Vessel Cannula Blunt Tip, Model Number 30004; b) DLP® ... | 2 | 05/10/2024 | Medtronic Perfusion Systems |
Medtronic DLP Vessel Cannula, Model Number REF 30000 | 2 | 03/19/2024 | Medtronic Perfusion Systems |
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