• 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 
 5 
 6 
 7 
 8 
 9 
 > 
 
85 records meeting your search criteria returned- Product Code: FMI Patient Problem: Underdose Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BECTON DICKINSON AND CO. BD AUTOSHIELD DUO SAFETY PEN NEEDLE 01/29/2020
BECTON DICKINSON UNSPECIFIED BD NEEDLE 01/27/2020
BECTON DICKINSON INFUSION THERAPY SYSTEM BD ULTRA FINE PEN NEEDLES 01/20/2020
BECTON DICKINSON AND CO. BD ULTRA-FINE¿ SHORT PEN NEEDLES 8MM (5/ 12/31/2019
BECTON, DICKINSON AND CO. BD ULTRA FINE¿ PEN NEEDLES 12/27/2019
BECTON DICKINSON AND CO. BD¿ PEN NDL 32G 4MM PRO 100 BOX AP 12/16/2019
BECTON DICKINSON UNSPECIFIED BD¿ PEN NEEDLE 12/10/2019
SMITHS MEDICAL ASD, INC. NEEDLE, HYPODERMIC, SINGLE LUMEN 11/22/2019
BECTON DICKINSON PEN II OMNITROPE PEN 10 11/21/2019
BECTON, DICKINSON AND CO. BD ULTRA FINE¿ INSULIN PEN NEEDLE 11/08/2019
-
-