MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-03-23 for PHILIPS RESPIRONICS V60 1053616 manufactured by Respironics California, Inc..
[184467191]
Patient was found with bipap mask off and machine was shut off and alarming. Machine would not turn back on. Machine continued to alarm when machine off.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9864912 |
MDR Report Key | 9864912 |
Date Received | 2020-03-23 |
Date of Report | 2020-02-12 |
Date of Event | 2020-01-17 |
Report Date | 2020-02-12 |
Date Reported to FDA | 2020-02-12 |
Date Reported to Mfgr | 2020-03-23 |
Date Added to Maude | 2020-03-23 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 0 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | RISK MANAGER |
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 | PHILIPS RESPIRONICS |
Generic Name | VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY USE |
Product Code | MNT |
Date Received | 2020-03-23 |
Model Number | V60 |
Catalog Number | 1053616 |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | RESPIRONICS CALIFORNIA, INC. |
Manufacturer Address | 2271 COSMOS CT CARLSBAD CA 92011 US 92011 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-23 |