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 
 
 
29 records meeting your search criteria returned- Product Code: FMK 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
ROCHE DIAGNOSTICS ACCU-CHEK SOFTCLIX LANCETS 10/27/2016
HTL-STREFA S.A. HAEMOLANCE PLUS MAX FLOW 09/21/2016
ASCENSIA DIABETES CARE US INC. MICROLET 03/09/2016
ROCHE DIABETES CARE, INC. SOFTCLIX ® LANCETS 07/07/2015
ABBOTT DIABETES CARE INC. FREESTYLE LANCET 04/09/2015
BAYER HEALTHCARE LLC MICROLET 09/26/2014
ROCHE DIAGNOSTICS ACCU-CHEK ® FASTCLIX LANCETS 09/04/2014
ROCHE DIAGNOSTICS SOFTCLIX ® LANCETS 06/18/2014
ROCHE DIAGNOSTICS SAFE-T-PRO PLUS 03/20/2014
-
-