FDA Adverse Event
Malfunction
Summary report: N
HEART START XL
MDR report key: 4182377
·
Received August 8, 2014
Report
- Report Number
- 1218950-2014-04724
- Event Type
- Malfunction
- Date Received
- August 8, 2014
- Report Date
- March 8, 2012
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Product Code
- MKJ
- PMA / PMN Number
- K001725
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SF
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
(B)(4).
Description of Event or Problem · 1
THE CUSTOMER CONTACTED PHILIPS HEALTHCARE TO REPORT THAT THE DEFIBRILLATOR DISPLAY WAS FLICKERING. THERE WAS NO REPORT OF PT INVOLVEMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 466830 | HEART START XL | MKJ | PHILIPS MEDICAL SYSTEMS | M4735A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |