MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-27 for CAREEVENT REL A.0 866435 manufactured by Philips Medical Systems.
[185472385]
A follow up report will be submitted once the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10
[185472386]
The customer nurse stated that a patient connected to a mx40 device in room 20b, unit 9e coded, and the alarm did not get paged to their cisco phones; the patient was declared dead on (b)(6) 2020, around 11:55 am. It was noted the alarms did go to the central station (pic ix).
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1218950-2020-01976 |
MDR Report Key | 9891146 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2020-03-27 |
Date of Report | 2020-03-26 |
Date of Event | 2020-03-26 |
Date Mfgr Received | 2020-03-26 |
Date Added to Maude | 2020-03-27 |
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 | MS. BETTY HARRIS |
Manufacturer Street | 3000 MINUTEMAN ROAD |
Manufacturer City | ANDOVER MA 01810 |
Manufacturer Country | US |
Manufacturer Postal | 01810 |
Manufacturer Phone | 9786871501 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CAREEVENT REL A.0 |
Generic Name | CARDIAC MONITOR |
Product Code | MSX |
Date Received | 2020-03-27 |
Model Number | 866435 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PHILIPS MEDICAL SYSTEMS |
Manufacturer Address | 3000 MINUTEMAN ROAD ANDOVER MA 01810 US 01810 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Death | 2020-03-27 |