A medical device correction is being issued for SIGMA Spectrum Infusion System (V8 Platform) and Spectrum IQ Infusion System with Dose IQ Safety Software infusion pumps due to an increase in reported false upstream occlusion alarms following upgrades to software versions v8.01.01 and v9.02.01.
Reason for recall: A medical device correction is being issued for SIGMA Spectrum Infusion System (V8 Platform) and Spectrum IQ Infusion System with Dose IQ Safety Software infusion pumps due to an increase in reported false upstream occlusion alarms following upgrades to software versions v8.01.01 and v9.02.01. Distribution: US Nationwide distribution. Quantity: 19861 units Lot/code info: UDI/DI 00085412610900, Software Version v9.02.01, All Serial Numbers
00085412610900
Official record: FDA (Device enforcement) ↗
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