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 
 4 
 > 
 
32 records meeting your search criteria returned- Product Code: KXG Product Problem: Defective Component Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CAREFUSION, INC CHLORAPREP ONE-STEP HI-LITE ORANGE 08/18/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI LITE ORANGE 07/15/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI LITE ORANGE 06/23/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI LITE ORANGE 06/23/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI LITE ORANGE 06/08/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI LITE ORANGE 05/04/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI LITE ORANGE 05/04/2021
CAREFUSION, INC CHLORAPREP ONE STEP HI LITE ORANGE 04/05/2021
CAREFUSION, INC CHLORAPREP ONE STEP HI LITE ORANGE 04/05/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI LITE ORANGE 03/16/2021
-
-