• 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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
150 records meeting your search criteria returned- Product Code: DXC Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
TERUMO MEDICAL CORPORATION TR BAND 01/06/2021
TERUMO MEDICAL CORPORATION TR BAND 11/19/2020
SYMMETRY SURGICAL INC CODMAN DEBAKEY 10/08/2020
BAXTER HEALTHCARE CORPORATION FLO-THRU 09/16/2020
BAXTER HEALTHCARE CORPORATION FLO-THRU 09/16/2020
BAXTER HEALTHCARE CORPORATION NI 08/24/2020
BAXTER HEALTHCARE CORPORATION FLO-THRU 08/19/2020
BAXTER HEALTHCARE CORPORATION FLO-THRU 08/19/2020
BAXTER HEALTHCARE CORPORATION FLO-THRU 08/18/2020
ST. JUDE MEDICAL PUERTO RICO, INC. FEMOSTOP GOLD 08/12/2020
-
-