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

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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
 
63 records meeting your search criteria returned- Product Code: MLV Product Problem: Improper or Incorrect Procedure or Method Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT MEDICAL AMPLATZER PFO OCCLUDER 08/08/2023
ABBOTT MEDICAL AMPLATZER SEPTAL OCCLUDER 08/04/2023
ABBOTT MEDICAL AMPLATZER TALISMAN PFO OCCLUDER 07/11/2023
ABBOTT MEDICAL AMPLATZER PFO OCCLUDER 06/19/2023
ABBOTT MEDICAL AMPLATZER PFO OCCLUDER 06/19/2023
ABBOTT MEDICAL AMPLATZER TALISMAN PFO OCCLUDER 06/15/2023
ABBOTT MEDICAL AMPLATZER TALISMAN PFO OCCLUDER 06/12/2023
ABBOTT MEDICAL AMPLATZER POST-INFARCT VSD OCCLUDER 05/15/2023
ABBOTT MEDICAL AMPLATZER TALISMAN PFO OCCLUDER 03/21/2023
ABBOTT MEDICAL AMPLATZER SEPTAL OCCLUDER 03/14/2023
-
-