NEUROVENT-P
Report
- Report Number
- 3006942548-2017-00003
- Event Type
- Malfunction
- Date Received
- December 19, 2017
- Date of Event
- November 1, 2017
- Report Date
- November 22, 2017
- Manufacturer
- RAUMEDIC AG
- Product Code
- GWM
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- OTHER
Narratives
MANUFACTURER STATEMENT: FOR EVALUATION OF THE MALFUNCTION DHR DOCUMENTS WERE REVIEWED. THEY DEMONSTRATE THAT THE CATHETER NEUROVENT-P (SN (B)(4)) MET SPECIFICATION DURING MANUFACTURING. FINAL INSPECTION OF THE FINISHED CATHETER WAS PASSED. THIS DEMONSTRATES THAT THE CATHETER HAS BEEN MANUFACTURED AND SOLD IN CONFORMANCE TO RELEVANT SPECIFICATIONS. FURTHERMORE RETURNED CATHETER WAS INVESTIGATED. THIS INVESTIGATION DEMONSTRATES THAT ONE WIRE IS TORN APART FROM THE SOLDERING PADS ON THE PCB. BASED ON KNOWLEDGE THAT THE FINAL INSPECTION OF THE FINISHED CATHETER WAS PASSED, THAT THE CATHETER WAS DELIVERED WITH PROPER FUNCTIONALITY AND IN CONSIDERATION OF THE RESULTS OF PERFORMED INVESTIGATION OF RETURNED CATHETER, THE TEAR-OFF OF THE WIRE IS CAUSED BY USER ERROR BY STRETCHING OF THE CATHETER DURING APPLICATION CONTRARY TO IFU.
AFTER IMPLANTATION OF THE CATHETER ICP COULD BE MONITORED FOR 6 HOURS. AFTERWARDS THE MEASUREMENT COULD NOT CONTINUED ALSO WITH USEAGE OF ANOTHER MPR 1 DATALOGGER. SO THE CATHETER HAS BEEN EXPLANTED. NO IMPLANTATION OF ANOTHER CATHETER HAS BEEN CONDUCTED. FAILURE OF CATHETER DID NOT RESULT IN AN ADDITIONAL MEDICATION OR OPERATION. HEALTH CONDITION OF THE PATIENT IS WELL.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 911463 | NEUROVENT-P | NEUROLOGICAL CATHETER | GWM | RAUMEDIC AG | 092946-001 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 5 YR |