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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 18 Results
Product: alaris Recall Date to: 08/17/2015
 
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Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housin... 1 08/14/2015 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, Infusion pump. software version 9.17 Product Usage: The Alaris PC unit... 2 06/16/2015 FEI # 2016493
CareFusion 303, Inc.
Alaris PC units, Model No. 8015. Infusion pump. 2 03/23/2015 FEI # 2016493
CareFusion 303, Inc.
Alaris Pump model 8100 with software version 9.1.18 and software upgrade kits with "Delay Until" Opt... 1 05/14/2014 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 8015, with version 9.12-Keyboard Processor and logic board assembly part numbe... 1 08/02/2013 FEI # 2016493
CareFusion 303, Inc.
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 Pump Module Model 8100 (formerly Medley Pump Module) Subsequent Product Code: FPA. The ... 1 08/17/2012 FEI # 2016493
CareFusion 303, Inc.
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