FDAFebruary 18, 2016device
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.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Terminated
Brands named
mckesson medical immagingmckessonmckesson medical
Recall history
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