MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-19 for V60 VENTILATOR manufactured by Respironics California, Inc.
        [184455034]
Date of event: (b)(6) 2020. Date of report: 19march2020.
 Patient Sequence No: 1, Text Type: N, H10
        [184455035]
It was reported that during use the ventilator had a "check vent: internal temperature high. " the patient was removed from the ventilator and placed on an alternate ventilator. The patient was not harmed or injured as a result of the reported event.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2031642-2020-00965 | 
| MDR Report Key | 9856348 | 
| Report Source | COMPANY REPRESENTATIVE,USER F | 
| Date Received | 2020-03-19 | 
| Date of Report | 2020-03-02 | 
| Date Mfgr Received | 2020-03-02 | 
| Device Manufacturer Date | 2013-07-16 | 
| 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 | 
| Device Availability | Y | 
| Device Age | DA | 
| 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 |