• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CERNER CORPORATIONCERNER MILLENNIUM POWERCHART EASYSCRIPTSOFTWARE

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC | Inspections
 

CERNER CORPORATION CERNER MILLENNIUM POWERCHART EASYSCRIPT SOFTWARE   Back to Search Results
Event Date 03/03/2006
Event Type  Malfunction  
Manufacturer Narrative

Cerner has distributed a priority review flash notification march 2006 to all potentially impacted client sites. The software notification includes a description of the issue and will advise clients a software correction is available, how to obtain the correction and to implement these software modifications into their production. A software modification has been developed and is available to address the issue for all sites that could be potentially impacted.

 
Event Description

The issue involves the easyscript requisition, used within the powerchart office and powerchart core systems. When you place an order in easyscript and value the prn reason field, remove it, sign and submit the order, the prescription requisition prints the label "prn:" on the requisition. The millennium applications display the correct information but the printed requisiton does not reflect the change in in prn status. Pts may not take medications that should be taken on a regular basis due to incorrect medication administration instructions. Cerner has not been made aware of any adverse pt care events that resulted from this issue.

 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameCERNER MILLENNIUM POWERCHART EASYSCRIPT
Type of DeviceSOFTWARE
Manufacturer (Section F)
CERNER CORPORATION
2800 rockcreek pkwy.
kansas city MO 64117
Manufacturer (Section D)
CERNER CORPORATION
2800 rockcreek pkwy.
kansas city MO 64117
Manufacturer Contact
shelley looby
2800 rockcreek parkway
kansas city , MI 64117
(816) 201 -1368
Device Event Key684565
MDR Report Key695436
Event Key661828
Report Number1931259-2006-00002
Device Sequence Number1
Product CodeMMH
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation Invalid Data
Remedial Action Modification/Adjustment
Type of Report Initial
Report Date 03/31/2006
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received03/31/2006
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? No Answer Provided
Was the Report Sent to FDA? No
Was Device Evaluated By Manufacturer? Yes
Date Device Manufactured12/01/2003
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 Invalid Data

-
-