MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-11-20 for VITAL SIGNS manufactured by Carefusion.
[92538494]
Patient Sequence No: 1, Text Type: N, H10
[92538495]
Rn tried to inflate disposable pressure bag for arterial line set up. Hole in the bag - leaking air; would not inflate. No harm to patient.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 7045559 |
MDR Report Key | 7045559 |
Date Received | 2017-11-20 |
Date of Report | 2017-10-26 |
Date of Event | 2017-10-23 |
Report Date | 2017-10-26 |
Date Reported to FDA | 2017-10-26 |
Date Reported to Mfgr | 2017-10-26 |
Date Added to Maude | 2017-11-20 |
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 | 2017-11-20 |
Operator | NURSE |
Device Availability | Y |
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 | 2017-11-20 |