Market Intelligence Resource | July 29, 2013
FDA Class 2 Recall Notice Picis ED PulsecheckEMR Software Application
July 29, 2013
In a July 29, 2013, notice on the U.S. Food and Drug Administration (FDA) website UnitedHealth Groups OptumInsight subsidiary reported that it was voluntarily recalling certain versions of its Picis ED PulseCheck electronic health record (EHR) software to repair a problem that caused manually entered physician notes to patient prescriptions to be omitted from the patient chart in the EHR. The problem affected the ED PulseCheck- 2015 software, versions 5.2 and 5.3, used by 35 organizations in 20 states. Picis has completed a routine software update that resolved the issue for all users . . .
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