FDA Adverse Event
Malfunction
Summary report: N
HEARTSTART MRX
MDR report key: 4924794
·
Received July 20, 2015
Report
- Report Number
- 1218950-2015-03856
- Event Type
- Malfunction
- Date Received
- July 20, 2015
- Report Date
- June 26, 2015
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Product Code
- MKJ
- PMA / PMN Number
- K031187
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- HEALTH PROFESSIONAL
Narratives
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT THE DEVICE CANNOT BOOT UP. THERE WAS NO PATIENT INVOLVEMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 468443 | HEARTSTART MRX | DEFIBRILLATOR | MKJ | PHILIPS MEDICAL SYSTEMS | M3535A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |