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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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63 records meeting your search criteria returned- Product Code: DWF Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
PERFUSION SYSTEMS DLP CARDIAC SUCTION TUBE 07/16/2018
PERFUSION SYSTEMS DLP CARDIAC SUCTION TUBE 07/16/2018
COOK VASCULAR INC. VITAL-PORT DETACHED SILICONE CATHETER TI 05/21/2018
COOK VASCULAR INC. VITAL-PORT DETACHED SILICONE CATHETER TI 05/16/2018
COOK VASCULAR INC. VITAL-PORT DETACHED SILICONE CATHETER TI 04/23/2018
MEDTRONIC, INC. AORTIC ROOT CANNULA 01/04/2018
COOK VASCULAR INC VITAL-PORT DETACHED SILICONE CATHETER TI 05/19/2017
SORIN GROUP USA, INC AORTIC ARCH CANNULAS 03/24/2017
MEDTRONIC PERFUSION SYSTEMS DLP AORTIC ROOT ANTEGRADE ANTEGRADE CA 10/25/2016
BARD PERIPHERAL VASCULAR, INC. BARD CAROTID BYPASS SHUNT, 10F 10/26/2015
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