EDM LUMBAR DRAINAGE KIT, OPEN TIP CATHETER
Report
- Report Number
- 2021898-2014-00177
- Event Type
- Death
- Date Received
- May 27, 2014
- Date of Event
- December 10, 2013
- Report Date
- April 28, 2014
- Manufacturer
- MEDTRONIC NEUROSURGERY
- Product Code
- GWM
- PMA / PMN Number
- K802100
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- PHYSICIAN
Narratives
THE PRODUCT WAS UNAVAILABLE FOR RETURN. THEREFORE, AN EVALUATION OF DEVICE PERFORMANCE WAS NOT POSSIBLE. INFORMATION REGARDING THE EXACT DATE OF PATIENT DEATH IS UNKNOWN. A REVIEW OF THE MANUFACTURING AND STERILIZATION RECORDS SHOWED NO ANOMALIES. ADDITIONAL DEVICE/PATIENT INFORMATION: IT WAS REPORTED TO MEDTRONIC NEUROSURGERY THAT THE DOCTOR IMPLANTED THE PRODUCT IN (B)(6) 2013. ACCORDING TO THE REPORT, THE CEREBROSPINAL FLUID WAS FOUND TO BE LESS BLOODY. THE REPORT STATED THAT ONE DAY AFTER IMPLANTATION, THE PATIENT GOT A FEVER AND IT WAS FOUND THAT THE CEREBROSPINAL FLUID TURNED PURULENT. REPORTEDLY, PER THE LAB TEST RESULTS, THE PROTEIN COUNT OF THE CEREBROSPINAL FLUID WAS VERY HIGH. (B)(4).
A GOOD FAITH EFFORT WILL BE MADE TO OBTAIN THE APPLICABLE INFORMATION RELEVANT TO THE REPORT. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.
IT WAS REPORTED TO MEDTRONIC NEUROSURGERY THAT THE PATIENT HAD A CEREBROSPINAL FLUID INFECTION AFTER IMPLANTATION OF THE DEVICE. ACCORDING TO THE REPORT, THE PATIENT¿S WBC COUNT WAS FOUND TO HAVE INCREASED. THE REPORT STATED THAT THE DOCTOR EXPLANTED THE PRODUCT AND TREATED THE PATIENT WITH AN ANTIBIOTIC. REPORTEDLY, THE PATIENT DIED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 310898 | EDM LUMBAR DRAINAGE KIT, OPEN TIP CATHETER | DEVICE, MONITORING, INTRACRANIAL PRESSURE | GWM | MEDTRONIC NEUROSURGERY | 207441165 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Death |