• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Medical Device Recalls

  • Print
  • Share
  • E-mail
-
1 to 10 of 18 Results
510(K) Number: K060124
 
 1 
 2 
 > 
Results per Page
New Searchexport reports to excelExport to Excel | HelpHelp
Product Description
Sort by Product Name [A-Z]
Sort by Product Name [Z-A]
Recall
Class
Sort by Recall Class [0-9]
Sort by Recall Class [9-0]
FDA Recall
Posting Date
Sort by Date Classified [0-9]
Sort by Date Classified [9-0]
Recalling Firm
Sort by Recalling Firm [A-Z]
Sort by Recalling Firm [Z-A]
Flixene Grafts >or= 6mm Intended for use in arterial vascular reconstruction, segmental bypass, and... 2 09/30/2013 Atrium Medical Corporation
FLIXENE, 7X80, 1GDS, GW. Single-Ended Slider GDS. 2 06/04/2024 Atrium Medical Corporation
FLIXENE, 7X50, 1GDS, STR. Single-Ended Slider GDS. 2 06/04/2024 Atrium Medical Corporation
FLIXENE, 7X50, 1GDS, GW. Single-Ended Slider GDS. 2 06/04/2024 Atrium Medical Corporation
FLIXENE, 7X40, 1GDS, GW. Single-Ended Slider GDS. 2 06/04/2024 Atrium Medical Corporation
FLIXENE, 7X30, 1GDS, GW. Single-Ended Slider GDS. 2 06/04/2024 Atrium Medical Corporation
FLIXENE, 6X50, 1GDS, STR. Single-Ended Slider GDS. 2 06/04/2024 Atrium Medical Corporation
FLIXENE, 6X50, 1GDS, GW. Single-Ended Slider GDS. 2 06/04/2024 Atrium Medical Corporation
FLIXENE, 6X40, 1GDS, GW. Single-Ended Slider GDS. 2 06/04/2024 Atrium Medical Corporation
FLIXENE, 6X30, 1GDS, STR. Single-Ended Slider GDS. 2 06/04/2024 Atrium Medical Corporation
-
-