MAUDE Adverse Event Report: CERNER CERNER POWERCHART; MEDICAL DEVICE DATA SYSTEM

Device Problem Loss of Data (2903)

Patient Problem No Information (3190)

Event Date 06/23/2017

Event Type  malfunction  

Event Description

Cerner powerchart has functionality to paste images into documents.When pasting a screen shot of an mri, the document silently truncates the image so that important clinical documentation is permanently lost.

• Brand Name: CERNER POWERCHART
• Type of Device: MEDICAL DEVICE DATA SYSTEM
• Manufacturer (Section D): CERNER; kansas city MO 64117
• MDR Report Key: 6669614
• MDR Text Key: 78577535
• Report Number: MW5070649
• Device Sequence Number: 1
• Product Code: OUG
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Physician
• Type of Report: Initial
• Report Date: 06/23/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 06/23/2017
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was Device Evaluated by Manufacturer?: No Information
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Outcome(s): Other
• Patient Age: 8 YR
• Patient Weight: 21