FDA Adverse Event
Malfunction
Summary report: N
EXTERNAL PADDLES
MDR report key: 2082819
·
Received April 29, 2011
Report
- Report Number
- 1218950-2011-01222
- Event Type
- Malfunction
- Date Received
- April 29, 2011
- Report Date
- April 4, 2011
- Manufacturer
- PHILIPS HEALTHCARE
- Product Code
- MKJ
- PMA / PMN Number
- K001725
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GM
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
(B)(4). THE CUSTOMER REPORTED A DEFECTIVE PADDLE SET. NO PT INVOLVEMENT WAS INDICATED. THIS COMPLAINT IS STILL BEING INVESTIGATED. A FOLLOW-UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.
Description of Event or Problem · 1
THE CUSTOMER REPORTED A DEFECTIVE PADDLE SET. NO PT INVOLVEMENT WAS INDICATED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | EXTERNAL PADDLES | MKJ | PHILIPS HEALTHCARE | M4746A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |