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 3 of 3 Results
510(K) Number: K910215
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]
System 1000 family of Hemodialysis Instruments, including the System 1000, TINA, AURORA and Altratou... 2 04/18/2006 FEI # 3000210122
Baxter Healthcare Renal Div
Baxter System 1000 Single Patient Hemodialysis Delivery System; Model SYS1000; all series 1000 instr... 2 12/02/2004 FEI # 3000210122
Baxter Healthcare Renal Div
Baxter System 1000 Single Patient Hemodialysis Delivery System; Model SYS1000; all series 1000 instr... 2 05/15/2003 FEI # 1416980
Baxter Healthcare Corp.
-
-