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 
 4 
 5 
 6 
 7 
 8 
 9 
 10 
 > 
 
91 records meeting your search criteria returned- Product Code: FPA Product Problem: Material Integrity Problem Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SMITHS MEDICAL ASD, INC. CADD ADMINISTRATION SET 12/14/2023
BAXTER HEALTHCARE CORPORATION CLEARLINK DUO-VENT CONTINU-FLO SOLUTION 11/27/2023
ST PAUL CADD ADMINISTRATION SET 10/12/2023
ST PAUL CADD ADMINISTRATION SET 10/12/2023
ST PAUL CADD ADMINISTRATION SET 10/11/2023
ST PAUL CADD EXTENSION SETS 08/28/2023
ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V TEGO® CONNECTOR 07/20/2023
BAXTER INTERNATIONAL INC. CLEARLINK/DUO-VENT 07/12/2023
BAXTER HEALTHCARE CORPORATION CLEARLINK/CONTINU-FLO/DUO-VENT 06/29/2023
ICU MEDICAL COSTA RICA LTD. PRIMARY PLUM SET, CLAVE SECONDARY PORT, 05/19/2023
-
-