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 
 > 
 
36 records meeting your search criteria returned- Product Code: FMF Product Problem: Therapeutic or Diagnostic Output Failure Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BECTON DICKINSON SYRINGE 04/25/2023
ELI LILLY AND COMPANY HUMAPEN ERGO II 07/14/2022
ELI LILLY AND COMPANY HUMAPEN LUXURA HALF DOSE PEN 04/20/2022
BECTON DICKINSON AND COMPANY BD INTEGRA SYRINGE 02/02/2021
ELI LILLY AND COMPANY HUMAPEN LUXURA HALF-DOSE PEN 02/01/2021
ELI LILLY AND COMPANY HUMAPEN ERGO II 12/14/2020
COMPANION MEDICAL INC INPEN 11/18/2020
ELI LILLY AND COMPANY HUMAPEN ERGO II 08/27/2020
ELI LILLY AND COMPANY HUMAPEN LUXURA BURGUNDY 08/27/2020
ELI LILLY AND COMPANY HUMAPEN SAVVIO 3ML (GRAY) 07/28/2020
-
-