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
 

 
 < 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
122 records meeting your search criteria returned- Product Code: LQL Product Problem: Incorrect Or Inadequate Test Results Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 03/03/2017
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 02/27/2017
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 02/22/2017
BIOMERIEUX, INC VITEK® 2 AST-GP67 TEST KIT 02/22/2017
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 02/13/2017
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 02/09/2017
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 02/09/2017
BIOMERIEUX, INC VITEK® 2 GRAM-POSITIVE IDENTIFICATION ID 02/02/2017
BIOMERIEUX, INC VITEK® 2 GP TEST KIT 02/01/2017
BIOMERIEUX, INC VITEK® 2 GP ID TEST KIT 01/31/2017
-
-