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
 

 
 < 
 2 
 3 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 11 
 > 
 
116 records meeting your search criteria returned- Product Code: FMI Product Problem: Mechanical Problem Report Date From: 01/1/2009

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BD SAFETYGLIDE NEEDLE 02/27/2019
BECTON DICKINSON MEDICAL (SINGAPORE) BD HYPOINT NEEDLE 02/18/2019
BECTON DICKINSON OMNITROPE® PEN 10 02/18/2019
BECTON DICKINSON PEN II OMNITROPE PEN 10 02/08/2019
BECTON DICKINSON AND CO. BD AUTOSHIELD¿ DUO SAFETY PEN NEEDLE 01/28/2019
BECTON DICKINSON UNSPECIFIED BD SAFETYGLIDE¿ NEEDLE 01/11/2019
BECTON DICKINSON MEDICAL (SINGAPORE) BD LUER-LOK¿ SYRINGE WITH DETACHABLE BD 12/31/2018
TRIVIDIA HEALTH, INC. PEN NEEDLE 12/27/2018
BECTON DICKINSON PEN II ORGANON PUREGON® PEN SECOND GEN 12/27/2018
TRIVIDIA HEALTH, INC. PEN NEEDLE 12/07/2018
-
-