Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K020271 |
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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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CentriMag Acute Circulatory Support System Motor, U.S. Model 102956 and OUS Model 201-10002, a compo... | 1 | 10/30/2019 | Thoratec Switzerland GMBH |
Thoratec CentriMag Motor, Model: 102956, a component of the Thoratec CentriMag Blood Pumping System ... | 2 | 10/12/2018 | Thoratec Switzerland GMBH |
Levitronix CentriMag Primary System, Article Number: 201-30100; extracorporeal blood circulation sy... | 1 | 07/23/2008 | Levitronix, Llc |
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