McKesson Cardiology Hemo software version 13.x has medication data discrepancies between procedure screens and patient records. Affected healthcare providers should verify medication data accuracy to prevent errors.
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.
McK:Cardiology Hemo software version 13.x has discrepancies in medication data between different screens. This could lead to incorrect medication records in reports, potentially affecting patient care.
The software shows medication discrepancies between procedure screens and patient data. This can cause incorrect medication records in reports, which might lead to wrong medication administration if not corrected.
Healthcare providers using McKesson Cardiology Hemo software version 13.x for patient records. Providers who generate medication reports are most at risk of data errors.
Check for software version 13.x on McKesson Cardiology Hemo. The product was sold to healthcare providers for patient record management.
Check your software version to confirm it is 13.x
The recall indicates potential medication data discrepancies, but it does not state that the software causes injury or serious harm.
Check for software version 13.x on McKesson Cardiology Hemo. The product was sold to healthcare providers for patient record management.
The recall does not specify a fix or action for discrepancies; users should verify data accuracy manually.
We’ve drafted a message you can send McKesson Cardiology Hemo to request your refund or repair — edit it as you like.
Subject: Recall Z-1490-2019 — McKesson Cardiology Hemo McKesson Cardiology Hemo Hello, I own a McKesson Cardiology Hemo that is covered by recall Z-1490-2019 from McKesson Cardiology Hemo. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
