MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-06-07 for PYXISES manufactured by Carefusion.
[47142900]
The pyxis es platform was implemented in our 6th hospital health system last year. The application is unstable and has resulted in hours/days of extended downtime, removing the electronic safety net that our clinicians rely on that scans patient and specific medication. This is a serious safety issue. We have learned that other health systems have had the same problems and carefusion is yet to give this sufficient attention.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5062755 |
| MDR Report Key | 5710346 |
| Date Received | 2016-06-07 |
| Date of Report | 2016-06-07 |
| Date Added to Maude | 2016-06-09 |
| 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 | PYXISES |
| Generic Name | PYXIS ES SOFTWARE |
| Product Code | BRY |
| Date Received | 2016-06-07 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CAREFUSION |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2016-06-07 |