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
 

 
 
8 records meeting your search criteria returned- Product Code: CFR Product Problem: Incorrect Or Inadequate Test Results Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT MANUFACTURING INC CLINICAL CHEMISTRY GLUCOSE 05/01/2018
ABBOTT MANUFACTURING INC CLINICAL CHEMISTRY GLUCOSE 12/01/2017
BECKMAN COULTER BECKMAN COULTER AU680 CLINICAL CHEMISTRY 08/28/2017
BECKMAN COULTER BECKMAN COULTER AU680 CLINICAL CHEMISTRY 08/28/2017
BECKMAN COULTER BECKMAN COULTER AU680 CLINICAL CHEMISTRY 08/28/2017
ROCHE DIAGNOSTICS COBAS INTEGRA 400 PLUS 06/30/2017
ROCHE DIAGNOSTICS GLUC3 GLUCOSE HK GEN.3 05/18/2017
ABBOTT MANUFACTURING INC CLINICAL CHEMISTRY GLUCOSE 05/10/2017
-
-