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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CERNER CORP.CERNER MILLENNIUM POWERCHART LOCAL ACCESSSOFTWARE

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CERNER CORP. CERNER MILLENNIUM POWERCHART LOCAL ACCESS SOFTWARE   Back to Search Results
Event Date 05/10/2006
Event Type  Malfunction  
Manufacturer Narrative

Cerner has distributed a priority review flash notification may 2006 to all potentially impacted client sites. The software notification includes a description of the issue and an interim workflow adjusment to prevent the malfunction. A software modification has been developed and is available to address the issue for all sites that could be potentially impacted. This issue is now considered resolved and no further narrative is necessary as follow up.

 
Event Description

The issue involves powerchart local access medication administration task, used when certain cerner millennium solutions are not available. At powerchart local access sites that utilize coordinated universal time (utc) functionality, medication administration tasks might be displayed with incorrect times. When a pt download occurs from cerner millennium servers to powerchart local access, and there is no cerner millennium application session active, powerchart local access adds or subtracts the number of hours equal to the time zone difference from greenwich mean time. Scheduled medication administration tasks may show an incorrect administration time and the possibility exists for a pt to receive medications earlier or later than intended. Since powerchart local access is a backup to a site's computer system, the clinician has no other source to view correct medication administration tasks. Cerner has not been made aware of any adverse pt care events that resulted from this issue.

 
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Brand NameCERNER MILLENNIUM POWERCHART LOCAL ACCESS
Type of DeviceSOFTWARE
Manufacturer (Section F)
CERNER CORP.
2800 rockcreek pkwy.
kansas city MO 64117
Manufacturer (Section D)
CERNER CORP.
2800 rockcreek pkwy.
kansas city MO 64117
Manufacturer Contact
shelley looby
2800 rockcreek parkway
kansas city , MO 64117
(816) 201 -1368
Device Event Key711684
MDR Report Key722614
Event Key688069
Report Number1931259-2006-00005
Device Sequence Number1
Product CodeLNX
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation Other
Remedial Action Modification/Adjustment
Type of Report Initial
Report Date 06/02/2006
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received06/02/2006
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator Health Professional
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? Yes
Was the Report Sent to FDA? No
Was Device Evaluated By Manufacturer? Yes
Date Device Manufactured07/01/2005
Is The Device Single Use? No
Is this a Reprocessed and Reused Single-Use Device? No
Is the Device an Implant? No
Is this an Explanted Device?
Type of Device Usage Unkown

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