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 
 > 
 
25 records meeting your search criteria returned- Product Code: FMF Product Problem: Device Displays Incorrect Message Report Date From: 01/1/2018
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
NOVO NORDISK A/S NOVOPEN ECHO PLUS 04/24/2023
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN ECHO 01/10/2023
NOVO NORDISK A/S NOVOPEN 6 06/27/2022
NOVO NORDISK A/S NOVOPEN ECHO PLUS 06/09/2022
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN ECHO 12/03/2021
HOSPIRA SYRINGE, PISTON 09/09/2021
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN ECHO 08/25/2021
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN ECHO 08/25/2021
BECTON DICKINSON UNSPECIFIED BD SYRINGE 07/15/2021
NOVO NORDISK A/S, MEDICAL SYSTEMS NOVOPEN ECHO 10/22/2020
-
-