• 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 
 > 
 
25 records meeting your search criteria returned- Product Code: MVR Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2016
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION NI 09/21/2021
BAXTER HEALTHCARE CORPORATION NI 09/21/2021
BAXTER HEALTHCARE CORPORATION NI 09/15/2021
BAXTER HEALTHCARE CORPORATION NI 09/08/2021
BAXTER HEALTHCARE CORPORATION NI 09/07/2021
BAXTER HEALTHCARE CORPORATION NI 09/07/2021
BAXTER HEALTHCARE CORPORATION FLOW COUPLER 03/08/2021
BAXTER HEALTHCARE CORPORATION COUPLER 02/15/2021
BAXTER HEALTHCARE CORPORATION COUPLER 11/09/2020
BAXTER HEALTHCARE CORPORATION FLOW COUPLER 10/15/2020
-
-