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

MAUDE - Manufacturer and User Facility Device Experience
  • 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 
 6 
 > 
 
55 records meeting your search criteria returned- Product Code: FPA Patient Problem: Overdose Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
CAREFUSION ALARIS PUMP MODULE ADMINISTRATION SET 04/21/2015
CAREFUSION ALARIS PUMP MODULE ADMINISTRATION SET 04/20/2015
CAREFUSION ALARIS PUMP MODULE ADMINISTRATION SET 04/06/2015
CAREFUSION SMARTSITE 1/2 INFUSION SET 12/24/2014
CAREFUSION CORP. ALARIS PUMP MODULE ADMINISTRATION SET 11/26/2014
CAREFUSION CORP ALARIS PUMP MODULE ADMINISTRATION SET 11/19/2014
CAREFUSION 303, INC SMARTSITE 10/14/2014
CAREFUSION CORP ALARIS PUMP MODULE ADMINISTRATION SET 05/30/2014
CAREFUSION 303,INC. VERSASAFE 05/29/2014
BAXTER HEALTHCARE ACCESS 05/23/2014
-
-