DURA DURATION A/P TIB LG 9
Report
- Report Number
- 0002249697-2014-03571
- Event Type
- Injury
- Date Received
- September 19, 2014
- Date of Event
- December 15, 2003
- Report Date
- August 25, 2014
- Manufacturer
- STRYKER ORTHOPAEDICS-MAHWAH
- Product Code
- MBH
- PMA / PMN Number
- K032163
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MD, US
- Reporter Occupation
- PHYSICIAN
Narratives
ADDITIONAL DEVICES LISTED IN THIS REPORT: CAT # 66300520, LOT # MNVI, DESCRIPTION: DCON STD BEADED FEM RHT L; CAT # 6632-3-630, LOT # MYGVA, DESCRIPTION: DURACON UNIVERSAL B/P NON-BEADED; CAT # 6642-2-150, LOT # 76413M, DESCRIPTION: DURA DURATION ALL POLY PAT LG. IT CANNOT BE DETERMINED WHICH, IF ANY OF THESE DEVICES MAY HAVE CAUSED OR CONTRIBUTED TO THE PATIENT'S EXPERIENCE. THE LOT CODE PROVIDED, 61203Y, IS INVALID. ADDITIONAL INFORMATION HAS BEEN REQUESTED AND IF RECEIVED, WILL BE PROVIDED IN THE SUPPLEMENTAL REPORT UPON COMPLETION OF THE INVESTIGATION.
THE PATIENT IS (B)(6) IN HEIGHT. AN EVENT REGARDING INFECTION INVOLVING A DURA DURATION A/P TIB LG 9 WAS REPORTED. THE EVENT WAS NOT CONFIRMED. CONCLUSIONS: THE SOURCE OF THE INFECTION COULD NOT BE DETERMINED AS PATIENT INFORMATION, CLINICAL HISTORY, AND RESULTS OF BLOODWORK FOR INFECTION WERE NOT PROVIDED. A CAPA TREND ANALYSIS WAS CONDUCTED FOR THE REPORTED FAILURE MODE AND CONCLUDED INFECTION IS MOST LIKELY A RESULT FROM OTHER FACTORS NOT NECESSARILY RELATED TO THE DEVICE IN THE HEALTHCARE FACILITY SETTING.
IT WAS REPORTED THAT PATIENT WAS REVISED DUE TO INFECTION.
IT WAS REPORTED THAT PATIENT WAS REVISED DUE TO INFECTION.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 583891 | DURA DURATION A/P TIB LG 9 | IMPLANT | MBH | STRYKER ORTHOPAEDICS-MAHWAH | UNKNOWN |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 52 YR | Hospitalization| R |