MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-19 for V60 VENTILATOR manufactured by Respironics California, Inc.
[186359042]
Date of event: (b)(6) 2020. Date of report: 19mar2020.
Patient Sequence No: 1, Text Type: N, H10
[186359043]
The customer reported a blue screen, and blower quitting. It is unknown if the ventilator was being used on a patient at the time that the error was discovered. Confirmation has been requested. The manufacturer? S field service engineer (fse) could not duplicate the issue. The fse remotely confirmed this was a unit that we were renting and was turned over to the rental company.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2031642-2020-00975 |
MDR Report Key | 9857900 |
Report Source | USER FACILITY |
Date Received | 2020-03-19 |
Date of Report | 2020-02-18 |
Date Mfgr Received | 2020-03-03 |
Device Manufacturer Date | 2015-06-25 |
Date Added to Maude | 2020-03-19 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
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 |
Manufacturer Contact | MRS. MELISSA ABBOTT |
Manufacturer Street | 2271 COSMOS COURT |
Manufacturer City | CARLSBAD CA 92011 |
Manufacturer Country | US |
Manufacturer Postal | 92011 |
Manufacturer Phone | 9093746996 |
Manufacturer G1 | PHILIPS MEDICAL SYSTEMS |
Manufacturer Street | 3000 MINUTEMAN ROAD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal Code | 01810 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | V60 VENTILATOR |
Generic Name | VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY USE |
Product Code | MNT |
Date Received | 2020-03-19 |
Model Number | V60 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | RESPIRONICS CALIFORNIA, INC |
Manufacturer Address | 2271 COSMOS COURT CARLSBAD CA 92011 US 92011 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-19 |