FDA Adverse Event
Malfunction
Summary report: N
MULTI DIAGNOST 4
MDR report key: 2180728
·
Received May 5, 2011
Report
- Report Number
- 3003768277-2011-00358
- Event Type
- Malfunction
- Date Received
- May 5, 2011
- Report Date
- April 5, 2011
- Manufacturer
- PHILIPS HEALTHCARE
- Product Code
- JAA
- PMA / PMN Number
- K961374
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NO
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
(B)(4). THE INVESTIGATION SHOWS THAT THE FIELD SVC ENGINEER TROUBLESHOT THE SYSTEM AND FOUND THAT THE RECTIFIER-FUSES WERE BAD. THE RECTIFIER FUSES WERE REPLACED AND THE ISSUE WAS RESOLVED.
Description of Event or Problem · 1
THE CUSTOMER REPORTED A BURNING SMELL IN THE LAB.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MULTI DIAGNOST 4 | JAA | PHILIPS HEALTHCARE | 708031 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |