FDA Adverse Event
Malfunction
Summary report: N
MP20 INTELLIVUE PATIENT MONITOR
MDR report key: 1890728
·
Received November 1, 2010
Report
- Report Number
- 9610816-2010-00566
- Event Type
- Malfunction
- Date Received
- November 1, 2010
- Report Date
- September 30, 2010
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Product Code
- MHX
- PMA / PMN Number
- K030038
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CT, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
(B)(4): THE CUSTOMER REPORTED THAT HIS MP20 SPEAKER WAS NOT WORKING AND HE REQUESTED A REPLACEMENT PART NUMBER. PHILIPS IS IN THE PROCESS OF OBTAINING ADDITIONAL INFORMATION CONCERNING THIS EVENT AND THE COMPLAINT IS STILL UNDER INVESTIGATION. A FINAL REPORT WILL BE SUBMITTED ONCE THE INVESTIGATION IS COMPLETED.
Description of Event or Problem · 1
THE CUSTOMER REPORTED THAT HIS MP20 SPEAKER WAS NOT WORKING AND HE REQUESTED A REPLACEMENT PART NUMBER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | MP20 INTELLIVUE PATIENT MONITOR | MHX | PHILIPS MEDICAL SYSTEMS | M8001A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |