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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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215 records meeting your search criteria returned- Product Code: KFM Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 05/24/2022
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 05/24/2022
THORATEC SWITZERLAND GMBH CMAG BLOOD PUMP 04/19/2022
CARDIACASSIST INC. TANDEMHEART PUMP 04/08/2022
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 04/01/2022
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 03/30/2022
THORATEC SWITZERLAND GMBH PEDIMAG BLOOD PUMP 03/28/2022
CARDIACASSIST INC. LIFESPARC SYSTEM 01/11/2022
THORATEC SWITZERLAND GMBH CENTRIMAG BLOOD PUMP 01/10/2022
THORATEC CORPORATION CENTRIMAG BLOOD PUMP 12/22/2021
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