• 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 
 > 
 
28 records meeting your search criteria returned- Product Code: KXG Product Problem: Manufacturing, Packaging or Shipping Problem Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI-LITE ORANGE 03/14/2022
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI-LITE ORANGE 03/11/2022
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI-LITE ORANGE 03/04/2022
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI-LITE ORANGE 11/01/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI-LITE ORANGE 11/01/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI-LITE ORANGE 10/17/2021
CAREFUSION 213, LLC 0113 CHLORAPREP UNKNOWN 09/21/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI-LITE ORANGE 08/11/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI-LITE ORANGE 08/04/2021
CAREFUSION 213, LLC 0113 CHLORAPREP ONE STEP HI-LITE ORANGE 07/28/2021
-
-