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Carefusion Corporation recalls Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming,
Recalled April 24, 2013 · FDA recall Z-1112-2013 · Carefusion
Hazard
The recall was initiated because Carefusion has identified potential risk associated with bolus programming with the Alaris PC unit (model 8015) software version 9.12. Automating infusion pump parameter input from either the electronic medical record (EMR) or the Alaris Auto-ID module for a continuous infusion with a bolus dose option may result in a loss of information from the Guardrails Data s · FDA Class II
Units
4,090 total units
Sold at
Worldwide Distribution USA Nationwide and the countries of Australia and Canada.
Description
The recall was initiated because Carefusion has identified potential risk associated with bolus programming with the Alaris PC unit (model 8015) software version 9.12. Automating infusion pump parameter input from either the electronic medical record (EMR) or the Alaris Auto-ID module for a continuous infusion with a bolus dose option may result in a loss of information from the Guardrails Data s
Product
Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and power supply component for the Alaris System
Manufacturer(s)
Carefusion Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →