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 6 of 6 Results
510(K) Number: K023264
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]
Alaris Syringe Pump, Model 8110. The firm name on the label is CareFusion. The Alaris Syringe Pu... 2 01/08/2018 CareFusion 303, Inc.
Alaris Syringe Module Model 8110 with software version 9.15 The Alaris Syringe Pump module is par... 2 09/23/2016 CareFusion 303, Inc.
Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housin... 1 08/14/2015 CareFusion 303, Inc.
Alaris System Inter-Unit Interface (IUI) Connectors. The Modules include the following: Alaris PC U... 1 08/03/2009 Cardinal Health 303 dba Cardinal Health
Grey Inter-Unit Interface Connectors ("IUI") on the following Alaris System modules built on or befo... 2 06/10/2008 Cardinal Health 303 Inc DBA Alaris Products
U9 Socket Integrated Circuit ("U9 IC") on the display board of the following Alaris System modules b... 2 06/10/2008 Cardinal Health 303 Inc DBA Alaris Products
-
-