FDA Adverse Event
Malfunction
Summary report: N
HEART START XL
MDR report key: 1874443
·
Received October 12, 2010
Report
- Report Number
- 1218950-2010-01931
- Event Type
- Malfunction
- Date Received
- October 12, 2010
- Report Date
- September 15, 2010
- Manufacturer
- PHILIPS HEALTHCARE
- Product Code
- MKJ
- PMA / PMN Number
- K001725
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- SP
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
(B)(4). ON (B)(6) 2010 THE CUSTOMER REPORTED THE PADDLE SET WAS INTERMITTENTLY DISCHARGING DURING TESTING. THIS COMPLAINT IS STILL BEING INVESTIGATED. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.
Description of Event or Problem · 1
ON (B)(6) 2010 THE CUSTOMER REPORTED THE PADDLE SET WAS INTERMITTENTLY DISCHARGING DURING TESTING.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HEART START XL | MKJ | PHILIPS HEALTHCARE | M4735A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |