Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K183623 |
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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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LifeSPARC Pump (part number 5800-0000) contained within TandemLife LifeSPARC Priming Tray part numb... | 2 | 08/25/2023 | Cardiac Assist, Inc |
SHIP KIT, LIFESPARC, CONTROLLER AND ACCESSORIES - 5900-0000; SHIP KIT, LIFESPARC, CONTROLLER ONLY ... | 1 | 01/19/2023 | Cardiac Assist, Inc |
TANDEM LIFE LivaNova LIFESPARC Controller; Controller and Accessories Model 5900-0000; Controller... | 1 | 09/23/2022 | Cardiac Assist, Inc |
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