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 
 5 
 
 
41 records meeting your search criteria returned- Product Code: FMI Product Problem: Improper Flow or Infusion Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
HTL-STREFA S.A. MEMBER'S MARK PEN NEEDLE 04/18/2019
BECTON DICKINSON UNSPECIFIED BD¿ SYRINGE 02/14/2019
BECTON DICKINSON AND CO. BD AUTOSHIELD¿ DUO PEN NEEDLE 09/12/2018
HTL - STREFA INC. NEEDLE 08/10/2018
BD INFUSION THERAPY SYSTEMS INC. S.A. DE BD NEXIVA¿ 18 GA X 1.25IN SP WITH MAXZER 07/26/2018
MHC MEDICAL PRODUCTS, LLC EASYTOUCH PEN NEEDLE 31G 5/16" (8MM) 06/13/2018
BECTON, DICKINSON & CO., (BD) BD ECLIPSE¿ BLOOD COLLECTION NEEDLE WITH 12/07/2017
BECTON DICKINSON AND CO. BD PEN NEEDLE 31G X 5MM 09/06/2016
RADIOMETER MEDICAL APS SAFEPICO 07/28/2016
BECTON, DICKINSON & CO., (BD) BD SAFETY-LOK BLOOD COLLECTION SET 23G N 05/03/2016
-
-