MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-01-22 for VITAL SIGNS manufactured by Carefusion.
[97904438]
Patient Sequence No: 1, Text Type: N, H10
[97904439]
Pressure bag for water bag on hfov not retaining air fill. Re-inflated x2 overnight but continued not to hold air. Bag re-inflated, but continued to lose air. Bag changed out and saved for risk management.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 7209564 |
| MDR Report Key | 7209564 |
| Date Received | 2018-01-22 |
| Date of Report | 2018-01-08 |
| Date of Event | 2018-01-07 |
| Report Date | 2018-01-08 |
| Date Reported to FDA | 2018-01-08 |
| Date Reported to Mfgr | 2018-01-08 |
| Date Added to Maude | 2018-01-22 |
| 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 | VITAL SIGNS |
| Generic Name | INFUSOR, PRESSURE, FOR I.V. BAGS |
| Product Code | KZD |
| Date Received | 2018-01-22 |
| Operator | NURSE |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | CAREFUSION |
| Manufacturer Address | 22745 SAVI RANCH PARKWAY YORBA LINDA CA 92887 US 92887 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-01-22 |