Medical Device Recalls
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1 result found
510(K) Number: K803277 |
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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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| RESERVOIR "Y" ADAPTER, (a) BT920 (b) BT926 Suction and Anticoagulation assemblies are indicate... | 2 | 01/29/2019 | Medtronic Perfusion Systems |
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