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 
 > 
 
13 records meeting your search criteria returned- Product Code: KZH Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MYLAN PHARMACEUTICALS INC. WHISPERJECT AUTOINJECTOR 05/16/2022
SCANDINAVIAN HEALTH LTD. GLATIRAMER ACETATE PREFILLED SYRINGE 40 07/14/2021
OWEN MUMFORD LIMITED AUTOJECT 2 FOR GLASS SYRINGE 02/14/2020
MYLAN PHARMACEUTICALS, INC. WHISPERJECT 01/16/2020
OWEN MUMFORD, LTD AUTOJECT DEVICE 12/23/2019
OWEN MUMFORD LIMITED AUTOJECT 2 FOR GLASS SYRINGE 10/08/2018
MEDTRONIC MINIMED LANCET DEVICE MMT-385 SILSRTR EA 13L 08/23/2018
MEDTRONIC MINIMED PARADIGM QUICKSERTER 09/18/2017
MEDTRONIC MINIMED LANCET DEVICE SNSRTR CMFRT EN 08/28/2015
MEDTRONIC MINIMED PARADIGM QUICKSERTER 12/20/2014
-
-