3(4/2019 MAUDE Adverse Event Report: EPIC CPOEIEHR

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MAUDE Adverse Event Re ort: EPIC 
Registration 8? lAdverse lRecalls11 
Listingg Events1U

 

CFR Title 2115lRadiation-Emitting Productlelx-Ray Assembler13 Medsun 

EPIC CPOEIEHR Back to Search Results
Event Date 06/01/2015

Event Type Injury

Event Description

The drop down menu to specify route of administration of medications is a source of innumerable errors. The first
option is im and is frequently selected because of its location and close resemblance to iv. It is a flaw that has been
carried on by the vendor for years, endangering hundreds of patients, if not thousands over time.

Search Alerts/Recalls22

New Search Submit an Adverse Event Report23

Brand 
Type of 
Manufacturer (Section 
Verona WI 53593
MDR Report Key4834779
Report NumberMW5043001
Device Sequence Numberl
Product Codew24
Report SourceVoiuntary
Reporter 
Type of Reportlnitial
Report Date06/03/2015
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received06/0312015
Is This An Adverse Event Report?No
Is This A Product Problem Report?Yes
Device OperatorHealth Professional
Is The Reporter A Health Professional?Yes
Is this a Reprocessed and Reused Single-Use Device?No

Patient TREATMENT DATA
Date Received: 06(03l2015 Patient Sequence Number: 1

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MAUDE Adverse Event Report: EPIC CPOEIEHR

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