Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
 
63 records meeting your search criteria returned- Product Code: DWF Product Problem: Detachment of Device or Device Component Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MAQUET CARDIOPULMONARY GMBH CATHETERS & CANNULAE 01/22/2020
COOK VANDERGRIFT INC VITAL-PORT DETACHED SILICONE CATHETER TI 12/11/2019
COOK VANDERGRIFT INC VITAL-PORT DETACHED SILICONE CATHETER TI 12/11/2019
MAQUET CARDIOPULMONARY GMBH CATHETERS & CANNULAE 12/02/2019
MAQUET CARDIOPULMONARY GMBH CATHETERS & CANNULAE 11/30/2019
MAQUET CARDIOPULMONARY GMBH CATHETERS & CANNULAE 11/30/2019
EDWARDS LIFESCIENCES QUICKDRAW VENOUS CANNULA 11/25/2019
EDWARDS LIFESCIENCES EZ GLIDE AORTIC CANNULA, AORTIC PERFUSIO 11/08/2019
MAQUET CARDIOPULMONARY GMBH CATHETERS & CANNULAE 10/17/2019
EDWARDS LIFESCIENCES PROPLEGE 10/11/2019
-
-