MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-08-19 for CERNER BRIDGE MEDPOINT manufactured by Cerner Bridge.
[1351668]
Error identified in (b)(4) -barcoding- database. On loading a new product in our formulary, the database autopopulated the "description" field with "epinephrine" for the pharmedium products for norepinephrine, (b)(4) and (b)(4). Our cerner bridge version is (b)(4) with database version (b)(4).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5017186 |
| MDR Report Key | 1813797 |
| Date Received | 2010-08-19 |
| Date of Report | 2010-08-19 |
| Date of Event | 2010-08-19 |
| Date Added to Maude | 2010-08-30 |
| 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 | 0 |
| Reporter Occupation | PHARMACIST |
| 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 |
| Brand Name | CERNER BRIDGE MEDPOINT |
| Generic Name | MEDPOINT SYSTEM MANAGER |
| Product Code | NZH |
| Date Received | 2010-08-19 |
| ID Number | DATABASE VERSION |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CERNER BRIDGE |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2010-08-19 |