• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • 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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
280 records meeting your search criteria returned- Product Code: LWR Product Problem: Torn Material Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, COSTA RICA LTDA SJM TRIFECTA VALVE 12/11/2017
ST. JUDE MEDICAL, COSTA RICA LTDA SJM TRIFECTA VALVE 12/08/2017
ST. JUDE MEDICAL, COSTA RICA LTDA SJM TRIFECTA VALVE 12/08/2017
ST. JUDE MEDICAL CANADA, INC. TRIFECTA VALVE 11/28/2017
ST. JUDE MEDICAL, COSTA RICA LTDA SJM TRIFECTA VALVE 11/22/2017
ST. JUDE MEDICAL, COSTA RICA LTDA (CVD) SJM TRIFECTA VALVE 11/14/2017
Unknown Manufacturer EPIC STENTED PORCINE HEART VALVE W/FLEXF 11/13/2017
MEDTRONIC HEART VALVE DIVISION HANCOCK II AORTIC CINCH 23 11/07/2017
ST. JUDE MEDICAL, BRASIL LTDA. (PAMPULHA EPIC STENTED PORCINE HEART VALVE W/FLEXF 10/15/2017
ST. JUDE MEDICAL, COSTA RICA LTDA SJM TRIFECTA VALVE 10/15/2017
-
-