• 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 25 Results
510(K) Number: K051641
 
 1 
 2 
 3 
 > 
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]
BD Alaris Syringe Module, REF 8110 1 11/07/2023 CareFusion 303, Inc.
BD Alaris PCU REF 8015 1 11/07/2023 CareFusion 303, Inc.
Alaris PCA Module 8120 1 11/07/2023 CareFusion 303, Inc.
CareFusion Alaris PCA Module, Model 8120 1 03/05/2020 CareFusion 303, Inc.
CareFusion Alaris Syringe Module, Model 8110 1 03/05/2020 CareFusion 303, Inc.
CareFusion Alaris Pump Module, Model 8100 1 03/05/2020 CareFusion 303, Inc.
Alaris PC Unit, Model 8015 2 06/19/2017 CareFusion 303, Inc.
Alaris System PC unit, model no. 8000 and 8015. The central programming, monitoring and power suppl... 2 03/21/2017 CareFusion 303, Inc.
Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19; Central programming, monitor... 2 06/28/2016 CareFusion 303, Inc.
Alaris PC unit, Model 8015 The Alaris PC unit is the central programming, monitoring and power su... 2 05/04/2016 CareFusion 303, Inc.
-
-