CERNER MILLENNIUM DYNAMIC DOCUMENTATION 2015.01 - 2018.01 N/A

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2018-05-14 for CERNER MILLENNIUM DYNAMIC DOCUMENTATION 2015.01 - 2018.01 N/A manufactured by Cerner Corporation.

Event Text Entries

[108254628] Cerner distributed a flash notification on (b)(6) 2018 to all potentially impacted client sites. The software notification includes a description of the issue, alternative workflows and a software modification is being developed to address the issue for all sites that could be potentially impacted. Cerner corporation will provide a follow-up report when the software modification is available.
Patient Sequence No: 1, Text Type: N, H10


[108254629] The software product mentioned in this medwatch report may not be, by definition, a medical device; however, cerner has chosen to file this medwatch report in order to voluntarily notify the fda of a malfunction associated with this software product. The company's filing of this medwatch report does not signify cerner's belief or understanding that medical device reports are required to be filed for products such as cerner's millennium dynamic documentation? , nor are these products currently actively regulated by the fda. This report documents information related to an issue identified with functionality included in cerner's millennium dynamic documentation? Medication reconciliation. The issue involves cerner millennium dynamic documentation and affects users that utilize medication reconciliation to create patients' discharge paperwork. In cerner millennium, the med_list_apply_org_security preference is not recognized when a user creates a note from a standard template. This preference allows an override of organizational security for medications and when this issue occurs, only medications that are within the current user's organizational security parameters will be displayed on the medication reconciliation. Medications outside the user's organizational parameters would be omitted. Patient care could be adversely affected if all medications are not displayed on the medication reconciliation as expected. This issue could result in patients not taking medication as prescribed. Cerner has not received communication on any adverse patient events as a result of this issue.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1931259-2018-00007
MDR Report Key7510185
Report SourceCOMPANY REPRESENTATIVE
Date Received2018-05-14
Date of Report2018-10-05
Date of Event2018-04-04
Date Mfgr Received2018-04-04
Device Manufacturer Date2015-12-17
Date Added to Maude2018-05-14
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. SHELLEY LOOBY
Manufacturer Street2800 ROCK CREEK PARKWAY
Manufacturer CityKANSAS CITY MO 64117
Manufacturer CountryUS
Manufacturer Postal64117
Manufacturer Phone8162011368
Manufacturer G1CERNER CORPORATION
Manufacturer Street2800 ROCK CREEK PARKWAY
Manufacturer CityKANSAS CITY MO 64117
Manufacturer CountryUS
Manufacturer Postal Code64117
Single Use3
Remedial ActionNO
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCERNER MILLENNIUM DYNAMIC DOCUMENTATION
Generic NameSOFTWARE
Product CodeLNX
Date Received2018-05-14
Model Number2015.01 - 2018.01
Catalog NumberN/A
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerCERNER CORPORATION
Manufacturer Address2800 ROCK CREEK PARKWAY KANSAS CITY MO 64117 US 64117


Patients

Patient NumberTreatmentOutcomeDate
10 2018-05-14

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