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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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11 records meeting your search criteria returned- Product Code: DWA Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
CARDIACASSIST INC. LIFESPARC SYSTEM 10/10/2023
CARDIACASSIST INC. LIFESPARC SYSTEM 09/19/2023
LIVANOVA DUTSCHLAND CENTRIFUGAL PUMP 5 (CP5) 08/13/2020
TERUMO CARDIOVASCULAR SYSTEMS CORPORATIO SARNS CENTRIFUGAL SYSTEM 01/09/2020
LIVANOVA DEUTSCHLAND CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAM 11/13/2019
LIVANOVA DEUTSCHLAND CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAM 11/12/2019
Unknown Manufacturer UNKNOWN 07/15/2019
LIVANOVA DEUTSCHLAND CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAM 06/06/2019
LIVANOVA DEUTSCHLAND CENTRIFUGAL PUMP 5 (CP5) 05/09/2019
LIVANOVA DEUTSCHLAND CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAM 03/12/2019
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