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 
 > 
 
56 records meeting your search criteria returned- Product Code: LJS Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BARD ACCESS SYSTEMS GROSHONG NXT CLEARVUE CATHETER WITH SHER 01/15/2018
BARD ACCESS SYSTEMS 4 FR. S/L POWERPICC - RADIOLOGY, STANDAR 12/14/2017
BARD ACCESS SYSTEMS GROSHONG NXT CLEARVUE 4F SINGLE-LUMEN BA 11/03/2017
BARD ACCESS SYSTEMS UNKNOWN CHRONIC CATHETER 10/25/2017
BARD ACCESS SYSTEMS POWERPICC SOLO2 CATHETER 4F MAXIMAL BARR 10/05/2017
BARD ACCESS SYSTEMS POWERPICC SOLO FT CATHETER WITH SHERLOCK 09/14/2017
BARD ACCESS SYSTEMS UNKNOWN HICKMAN CATHETER 08/18/2017
BARD ACCESS SYSTEMS UNKNOWN HICKMAN CATHETER 08/18/2017
BARD ACCESS SYSTEMS UNKNOWN HICKMAN CATHETER 08/18/2017
BARD ACCESS SYSTEMS POWERPICC CATHETER WITH SHERLOCK 3CG (TP 07/27/2017
-
-