MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-11-23 for PYXIS ES manufactured by Carefusion 303, Inc..
[31940536]
Patient Sequence No: 1, Text Type: N, H10
[31940537]
Pyxis es med station power failure. Could not dispense meds from pyxis.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 5243504 |
| MDR Report Key | 5243504 |
| Date Received | 2015-11-23 |
| Date of Report | 2015-11-19 |
| Date of Event | 2015-10-08 |
| Report Date | 2015-11-19 |
| Date Reported to FDA | 2015-11-19 |
| Date Reported to Mfgr | 2015-11-19 |
| Date Added to Maude | 2015-11-23 |
| Event Key | 0 |
| Report Source Code | User Facility 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 | 3 |
| Brand Name | PYXIS ES |
| Generic Name | CABINET, TABLE AND TRAY, ANESTHESIA, MEDICATION DISPENSING |
| Product Code | BRY |
| Date Received | 2015-11-23 |
| Model Number | ES |
| Device Availability | Y |
| Device Age | 1 DY |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CAREFUSION 303, INC. |
| Manufacturer Address | 10020 PACIFIC MESA BLVD. SAN DIEGO CA 92121 US 92121 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2015-11-23 |