• 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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
275 records meeting your search criteria returned- Product Code: FPA Product Problem: Air Leak Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
MEDTRONIC MINIMED SOF SET ULTIMATE 03/07/2016
MEDTRONIC MINIMED PARADIGM POLYFIN 03/04/2016
MEDTRONIC MINIMED SOF SET ULTIMATE 03/04/2016
CAREFUSION 303, INC. SMARTSITE PRIMARY INFUSION IV SET 02/02/2016
CAREFUSION ALARIS PUMP MODULE ADMINISTARTION SET 01/25/2016
CAREFUSION SMARTSITE INFUSION SET 01/22/2016
BAXTER HEALTHCARE - MALTA ACCESS 01/21/2016
CAREFUSION 303, INC. SET, ADMINISTRATION, INTRAVASCULAR 01/15/2016
B. BRAUN DOMINICAN REPUBLIC INC. INFUSOMAT® SPACE PUMP SETS WITH CARESITE 01/12/2016
B. BRAUN DOMINICAN REPUBLIC INC. BLOOD SETS WITH CARESITE INJECTION SITES 01/07/2016
-
-