MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2018-04-11 for CERNER MILLENNIUM REGISTRATION MANAGEMENT 2015.01 - 2018.01 N/A manufactured by Cerner Corporation.
[105645731]
Cerner distributed a flash notification on april 6, 2018 to all potentially impacted client sites. The software notification includes a description of the issue and explains that 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
[105645732]
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 registration management? , 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 registration management. This issue involves cerner millennium registration management and occurs when a new encounter is added for a patient that already has an existing encounter with an mrn during a rolling upgrade. When this occurs, a new, additional mrn is assigned to the encounter when it is saved. The additional mrn is assigned to the new encounter, and is displayed on registration documents (such as armbands and facesheets) and in cerner millennium? Powerchart?. If the mrn in the encounter was modified, the original mrn is displayed in the encounter but both mrns are displayed inconsistently throughout cerner millennium and on associated printed documents. This issue could lead to a delay in patient care if the mrn associated to an order (i. E. Medication, blood product, etc. ) did not match the information on the patient's armband or other patient identifiers presented. Cerner has not received communication on adverse patient events as a result of this issue.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1931259-2018-00004 |
| MDR Report Key | 7421951 |
| Report Source | COMPANY REPRESENTATIVE |
| Date Received | 2018-04-11 |
| Date of Report | 2018-08-03 |
| Date of Event | 2018-03-04 |
| Date Mfgr Received | 2018-03-14 |
| Device Manufacturer Date | 2017-04-06 |
| Date Added to Maude | 2018-04-11 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. SHELLEY LOOBY |
| Manufacturer Street | 2800 ROCK CREEK PARKWAY |
| Manufacturer City | KANSAS CITY MO 64117 |
| Manufacturer Country | US |
| Manufacturer Postal | 64117 |
| Manufacturer Phone | 8162011368 |
| Manufacturer G1 | CERNER CORPORATION |
| Manufacturer Street | 2800 ROCK CREEK PARKWAY |
| Manufacturer City | KANSAS CITY MO 64117 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 64117 |
| Single Use | 3 |
| Remedial Action | NO |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | CERNER MILLENNIUM REGISTRATION MANAGEMENT |
| Generic Name | SOFTWARE |
| Product Code | LNX |
| Date Received | 2018-04-11 |
| Model Number | 2015.01 - 2018.01 |
| Catalog Number | N/A |
| Lot Number | N/A |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CERNER CORPORATION |
| Manufacturer Address | 2800 ROCK CREEK PARKWAY KANSAS CITY MO 64117 US 64117 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-04-11 |