MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2008-07-03 for MCKESSON HBOC PHARMACY SYSTEM CONNECT RX 6.7.5.5 manufactured by Mckesson.
[878553]
Pharmacy tech was able to over-ride computer system passcode protection enabling him to remove controlled medications by changing their status. Mckesson unaware of this potential, advised of same in 2008. Employee terminated for drug diversion.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5007520 |
| MDR Report Key | 1069878 |
| Date Received | 2008-07-03 |
| Date of Report | 2008-07-03 |
| Date of Event | 2008-05-19 |
| Date Added to Maude | 2008-07-15 |
| 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 |
| Reporter Occupation | RISK MANAGER |
| 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 | MCKESSON HBOC PHARMACY SYSTEM |
| Generic Name | MCKESSON HBOC |
| Product Code | NZH |
| Date Received | 2008-07-03 |
| Model Number | CONNECT RX 6.7.5.5 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Implant Flag | N |
| Date Removed | B |
| Device Sequence No | 1 |
| Device Event Key | 1041385 |
| Manufacturer | MCKESSON |
| Manufacturer Address | SAN FRANCISO CA US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2008-07-03 |