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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 > 
 
128 records meeting your search criteria returned- Product Code: FJS Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COVIDIEN MFG SOLUTIONS S.A. DIALYSIS UNKNOWN 04/15/2022
COVIDIEN MFG SOLUTIONS S.A. DIALYSIS UNKNOWN 02/14/2022
COVIDIEN MFG SOLUTIONS S.A. DIALYSIS UNKNOWN 12/16/2021
MERIT MEDICAL SYSTEMS INC. PERITONEAL DIALYSIS CATHETER 07/17/2020
COVIDIEN MFG SOLUTIONS S.A. CATHETER, PERITONEAL, LONG-TERM INDWELLI 09/13/2018
COVIDIEN MFG SOLUTIONS S.A. CATHETER, PERITONEAL, LONG-TERM INDWELLI 07/03/2018
COVIDIEN MFG SOLUTIONS S.A. unknown brand name 05/09/2018
COVIDIEN MFG SOLUTIONS S.A. PERITONEAL 04/11/2018
COVIDIEN MFG SOLUTIONS S.A. PERITONEAL 04/10/2018
COVIDIEN MFG SOLUTIONS S.A. ARGYLE 01/31/2018
-
-