FDA Adverse Event
Malfunction
Summary report: N
CODEMASTER XL
MDR report key: 3221528
·
Received July 1, 2013
Report
- Report Number
- 1218950-2013-02753
- Event Type
- Malfunction
- Date Received
- July 1, 2013
- Report Date
- June 5, 2013
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Product Code
- LDD
- PMA / PMN Number
- K954957
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- BE
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
(B)(4). A FOLLOW UP REPORT WILL BE SUBMITTED UPON COMPLETION OF THE INVESTIGATION.
Description of Event or Problem · 1
THE CUSTOMER REPORTED DEFECTIVE BATTERIES. THERE WAS NO PATIENT INVOLVEMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 297433 | CODEMASTER XL | MKJ, DQA | LDD | PHILIPS MEDICAL SYSTEMS | M1723A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |