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: DQY Product Problem: Defective Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC IRELAND SYMPLICITY SPYRAL CATH RDN016 04/24/2024
MEDTRONIC IRELAND TELESCOPE GUIDE EXTENSION CATHETER 04/16/2024
BOSTON SCIENTIFIC CORPORATION ACUITY PRO 03/26/2024
BOSTON SCIENTIFIC CORPORATION GUIDEZILLA II 02/27/2024
MEDTRONIC IRELAND DEFLECT 02/15/2024
BOSTON SCIENTIFIC CORPORATION GUIDEZILLA II 02/06/2024
MEDTRONIC IRELAND DEFLECT 07/17/2023
MEDTRONIC, INC LAUNCHER 6F GUIDE CATHETER 07/06/2023
STRYKER NEUROVASCULAR EXCELSIOR XT-27 STD STRAIGHT 150CM 06/07/2023
BAYLIS MEDICAL COMPANY INC. TORFLEX TRANSSEPTAL GUIDING SHEATH 04/27/2023
-
-