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 
 > 
 
21 records meeting your search criteria returned- Product Code: OJX Product Problem: Defective Device Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKSITE LV 04/11/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKFLEX LV LEAD 03/29/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKFLEX LV LEAD 03/16/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKFLEX LV LEAD 03/13/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKSITE LV 02/27/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKFLEX LV LEAD 02/22/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKFLEX LV LEAD 02/17/2023
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKFLEX LV LEAD 12/20/2022
MPRI ATTAIN ABILITY MRI SURESCAN 06/22/2022
ST. JUDE MEDICAL, INC.(CRM-SYLMAR) QUICKFLEX XL LV LEAD 04/28/2022
-
-