MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-06-13 for EPIC EHR manufactured by Epic Systems Corporation.
[77718175]
There was a misidentification of the primary and private physician of this case that resulted in pt info and data being sent to the wrong physician, and a delay in it being distributed to the correct care team. Not only is this a hipaa violation, but it delays care upon transition from hospital. The ehr renders it difficult, if not impossible to, correct the error that populates many fields.
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5070405 |
MDR Report Key | 6642848 |
Date Received | 2017-06-13 |
Date of Report | 2017-06-13 |
Date of Event | 2017-06-10 |
Date Added to Maude | 2017-06-15 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
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 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | EPIC EHR |
Generic Name | EPIC SOFTWARE TRANSMISSION AND STORAGE |
Product Code | MMH |
Date Received | 2017-06-13 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | I |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | EPIC SYSTEMS CORPORATION |
Manufacturer Address | VERONA WI 53593 US 53593 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2017-06-13 |