MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-01-21 for ELECTRONIC MEDICAL RECORD manufactured by Epic.
[5318643]
Critically ill pt in resuscitation. Orders could not be entered in (b)(6) system because chart was open elsewhere in the facility. It services stated they could do nothing to correct the problem. Deadlock was eventually resolved, but not by specific action (other user eventually relinquished the chart).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5040484 |
| MDR Report Key | 4466577 |
| Date Received | 2015-01-21 |
| Date of Report | 2015-01-21 |
| Date of Event | 2015-01-21 |
| Date Added to Maude | 2015-01-30 |
| 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 | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Generic Name | ELECTRONIC MEDICAL RECORD |
| Product Code | NSX |
| Date Received | 2015-01-21 |
| Operator | HEALTH PROFESSIONAL |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | EPIC |
| Manufacturer Address | VERONA |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2015-01-21 |