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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
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67 records meeting your search criteria returned- Product Code: LWR Product Problem: Microbial Contamination of Device Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
EDWARDS LIFESCIENCES LLC EDWARDS INSPIRIS RESILIA AORTIC VALVE 01/24/2024
EDWARDS LIFESCIENCES LLC EDWARDS INSPIRIS RESILIA AORTIC VALVE 01/16/2024
EDWARDS LIFESCIENCES LLC KONECT RESILIA AORTIC VALVED CONDUIT AVC 01/07/2024
EDWARDS LIFESCIENCES LLC KONECT RESILIA AORTIC VALVED CONDUIT AVC 12/13/2023
EDWARDS LIFESCIENCES LLC EDWARDS INSPIRIS RESILIA AORTIC VALVE 10/09/2023
EDWARDS LIFESCIENCES LLC EDWARDS INSPIRIS RESILIA AORTIC VALVE 10/05/2023
EDWARDS LIFESCIENCES LLC INSPIRIS RESILIA AORTIC VALVE 29 MM BOVI 10/25/2022
ST. JUDE MEDICAL, COSTA RICA LTDA (CVD) TRIFECTA¿ GT VALVE 01/15/2020
ST. JUDE MEDICAL, COSTA RICA LTDA TRIFECTA¿ GT VALVE 12/23/2019
ST. JUDE MEDICAL, COSTA RICA LTDA TRIFECTA STENTED TISSUE VALVE 09/24/2019
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