• 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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
485 records meeting your search criteria returned- Product Code: FPA Product Problem: Defective Device Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SISTEMAS MEDICOS ALARIS, S.A. DE C.V. BD MAXPLUS PRESSURE RATED EXTENSION SET 05/18/2023
NEXUS MEDICAL, LLC MALE/FEMALE RED END CAPS 05/17/2023
SMITHS MEDICAL ASD, INC. CADD EXTENSION SET 05/11/2023
CAREFUSION 303, INC. BD MAXZERO 05/10/2023
BAXTER HEALTHCARE CORPORATION BAXTER ONE-LINK NEEDLE FREE IV CONNECTOR 05/04/2023
UNOMEDICAL A/S INF SET QUICK SET23" 9MM 05/01/2023
ICU MEDICAL, INC. SPINNING SPIROS CLOSED MALE LUER 04/20/2023
BAXTER INTERNATIONAL INC. ONE-LINK 03/30/2023
BAXTER HEALTHCARE CORPORATION CLEARLINK/CONTINU-FLO 03/24/2023
Unknown Manufacturer AUTOSOFT XC 02/26/2023
-
-