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

Medical Device Recalls
  • Print
  • Share
  • E-mail
-
1 to 5 of 5 Results
510(K) Number: K964850
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]
Baxter Interlink System Minivolume Extension Set, product code 1C8462; An Rx sterile, nonpyrogenic f... 2 03/24/2006 Baxter Healthcare Corp.
Baxter Interlink System Minivolume Extension Set, product code 1C8483; An Rx sterile, nonpyrogenic f... 2 03/24/2006 Baxter Healthcare Corp.
Baxter Interlink System Minivolume Extension Set, product code 1C8740; An Rx sterile, nonpyrogenic f... 2 03/24/2006 Baxter Healthcare Corp.
Baxter Interlink System Minivolume Extension Set, product code 1C8462; 16'', 4.2 mL Vol., with 0.22 ... 2 08/06/2005 Baxter Healthcare Corp.
Continu-Flo Solution Set, 10 drops/mL, 104'', 0.22 Micron Downstream High Pressure Extended Life Fil... 2 08/21/2003 Baxter Healthcare Corp.
-
-