medical Class II Updated 2019-06-05

Change Healthcare Israel Ltd. recalls McKesson Cardiology Hemo

Recalled Product

McKesson Cardiology Hemo

Hazard / Issue

users are not notified of procedure medication discrepancies between the Vitals and Meds, the Procedure Notes and Patient Common Data screens in Horizon/McKesson Cardiology Hemo" (Hemo). The discrepancy may also affect administered medication data in reports generated from Hemo or the Horizon/McKesson Cardiology Physician s Report as well as customers, who have implemented an outbound interface of procedure results.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Software version 13.x
View official government recall

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