ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT - 10886704075486
Report
- Report Number
- 1226348-2016-10313
- Event Type
- Injury
- Date Received
- April 20, 2016
- Manufacturer
- CODMAN & SHURTLEFF, INC.
- Product Code
- GWM
- PMA / PMN Number
- PN/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
Narratives
(B)(4).
A 510 (K) NUMBER FOR SIMILAR PRODUCT CODE OF 826638: K974088. (B)(4). IT HAS BEEN COMMUNICATED THAT THE DEVICE IS NOT AVAILABLE FOR EVALUATION. WITHOUT THE DEVICE IT IS NOT POSSIBLE FOR CODMAN TO CONDUCT A PROPER INVESTIGATION. SINCE A LOT NUMBER HAS BEEN PROVIDED A REVIEW OF THE MANUFACTURING RECORDS WILL BE REVIEWED. WE ANTICIPATE THAT THE EVALUATION WILL REVEAL THAT THE DEVICE CONFORMED TO SPECIFICATIONS PRIOR TO RELEASE. IF ANYTHING OTHERWISE IS FOUND THEN A FOLLOW UP REPORT WILL BE FILED. IF AT SOME POINT THE DEVICE DOES BECOME AVAILABLE, THIS COMPLAINT WILL BE RE-OPENED, EVALUATED AND A FOLLOW UP REPORT WILL BE FILED. TRENDS WILL BE MONITORED FOR THIS AND SIMILAR COMPLAINTS. AT THE PRESENT TIME THIS COMPLAINT IS CONSIDERED CLOSED. DEVICE NOT AVAILABLE.
THE SENSOR HAS FUNCTIONED CORRECTLY DURING A FEW DAYS BEFORE SHOWING NEGATIVE VALUES OR UNUSUAL FLUCTUATION . THE ZEROING PROCEDURE WAS CORRECT AND DIFFERENT ICP MONITORS WERE TESTED WHEN THE VALUES WERE FALSE. NO CLINICAL CONSEQUENCE. PATIENT RISK IF THE MONITORING HAS TO BE CHANGED
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 243319 | ROHS MICROSENSOR W/SINGLE LUMEN METAL BOLT KIT - 10886704075486 | DEVICE, INTRACRANIAL PRESSURE MONITORING | GWM | CODMAN & SHURTLEFF, INC. | CTKCCN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |