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
-
11 to 17 of 17 Results
510(K) Number: K051641
 < 
 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]
Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the ce... 1 04/15/2013 FEI # 3003879246
Carefusion Corporation
Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the ... 2 04/15/2013 FEI # 3003879246
Carefusion Corporation
Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only. 1 07/26/2012 FEI # 2016493
CareFusion 303, Inc.
Alaris PC unit model 8000 and 8015 with Alaris PCA module model 8120 and Auto ID barcode scanner mod... 1 12/20/2013 FEI # 2016493
CareFusion 303, Inc.
Alaris PC unit Model 8000 only when used with Alaris Pump module or Alaris Syringe module 2 06/26/2015 FEI # 2016493
CareFusion Corporation
Alaris PC Unit, Model 8015 2 06/19/2017 FEI # 2016493
CareFusion 303, Inc.
Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092 2 03/24/2016 FEI # 2016493
CareFusion 303, Inc.
-
-