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
 

 
 < 
 1 
 2 
 3 
 4 
 > 
 
37 records meeting your search criteria returned- Product Code: PZE Patient Problem: Fainting Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 14 DAY 06/08/2020
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 14 DAY 02/06/2020
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 14 DAY 01/29/2020
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 14 DAY 01/20/2020
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 14 DAY 01/09/2020
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 14 DAY 12/13/2019
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 14 DAY 11/18/2019
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 14 DAY 09/12/2019
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 14 DAY 09/04/2019
ABBOTT DIABETES CARE INC FREESTYLE LIBRE 14 DAY 08/29/2019
-
-