Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1182-2016 — McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products 12.0 and 12.1.1.

U.S. FDA — Device Enforcement · Canada · 2016-02-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1182-2016
Date of alert
2016-02-18
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
Mckesson Medical Immaging
Product category
device
Product type
Devices
Reported risk: McKesson has identified a design deficiency where under rare circumstances, imported images/studies may re-use a non-unique image directory. This issue may cause incorrect images to be displayed for a patient.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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