MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2006-05-25 for MEDITECH SYSTEM * manufactured by Meditech Information Tech, Inc..
[18598345]
A hospital has in place bar coded bedside medication verification and an electronic mar, all through their meditech system. Meditech electronic charting has this quirk where it will allow you to "administer" and chart a drug into the future, meaning that you could, for example, chart today that you "gave" next monday's dose already. Then when next monday rolls around, that dose never comes up on the emar to be administered because that day and time has already been satisfied as "given. " error did not reach the pt.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1039846 |
| MDR Report Key | 752527 |
| Date Received | 2006-05-25 |
| Date of Report | 2006-01-14 |
| Date Added to Maude | 2006-08-22 |
| 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 | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | MEDITECH SYSTEM |
| Generic Name | * |
| Product Code | NZH |
| Date Received | 2006-05-25 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Device Availability | N |
| Device Age | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 740329 |
| Manufacturer | MEDITECH INFORMATION TECH, INC. |
| Manufacturer Address | * * * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2006-05-25 |