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 
 
 
11 records meeting your search criteria returned- Product Code: DYE Product Problem: Device Dislodged or Dislocated Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
EDWARDS LIFESCIENCES CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL 01/16/2024
EDWARDS LIFESCIENCES CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRA 01/12/2024
EDWARDS LIFESCIENCES CARPENTIER-EDWARDS PERIMOUNT MAGNA MITRA 01/03/2024
MEDTRONIC HEART VALVES DIVISION MEDTRONIC SURGICAL TISSUE VALVE 01/27/2023
EDWARDS LIFESCIENCES CARPENTIER-EDWARDS PERIMOUNT MAGNA EASE 12/21/2018
EDWARDS LIFESCIENCES CARPENTIER-EDWARDS PERIMOUNT RSR PERICAR 08/09/2018
LIVANOVA CANADA CORP. PERCEVAL SUTURELESS AORTIC HEART VALVE 11/25/2016
LIVANOVA CANADA CORP. PERCEVAL SUTURELESS AORTIC HEART VALVE 11/04/2016
LIVANOVA CANADA CORP. PERCEVAL SUTURELESS AORTIC HEART VALVE 11/04/2016
LIVANOVA CANADA CORP. PERCEVAL SUTURELESS AORTIC HEART VALVE 10/28/2016
-
-