TL PEDICLE SCREW DIA. 6,5 LG 35
Report
- Report Number
- 3003853072-2019-00061
- Event Type
- Malfunction
- Date Received
- July 9, 2019
- Date of Event
- May 30, 2019
- Report Date
- February 4, 2020
- Manufacturer
- ZIMMER SPINE
- Product Code
- HWC
- PMA / PMN Number
- N/A
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- PHYSICIAN
Narratives
THE RETURNED DEVICE WAS EVALUATED. THERE WAS NO FAILURE MODE DETECTED. THE COMPLAINT IS NOT CONFIRMED.
THIS DEVICE IS NOT CLEARED IN THE US. IT IS SIMILAR TO PRODUCT CODE NKB CLEARED UNDER K111301. UDI NUMBER: NI. WITHOUT A PRODUCT RETURN, NO PRODUCT EVALUATION IS ABLE TO BE CONDUCTED. CURRENT INFORMATION IS INSUFFICIENT TO PERMIT A VALID CONCLUSION ABOUT THE CAUSE OF THIS EVENT. IF ADDITIONAL INFORMATION IS OBTAINED THAT ADDS VALUE TO THE RELEVANT CONTENT OF THIS REPORT AND/OR A CONCLUSION CAN BE DRAWN, A FOLLOW-UP REPORT WILL BE SENT. REFERENCE REPORTS: 3003853072-2019-00058 THRU 3003853072-2019-00071.
IT WAS REPORTED THAT THE THREADS OF 12 SCREWS AND 2 BLOCKERS WERE DAMAGED DURING INSTALLATION IN SURGERY. THEY WERE REMOVED AND REPLACED WITH ALTERNATIVE SCREWS AND BLOCKERS TO COMPLETE THE PROCEDURE WITHOUT REPORTED PATIENT IMPACTS. THIS IS REPORT 4 OF 14 FOR THIS EVENT.
IT WAS REPORTED THAT THE THREADS OF 12 SCREWS AND 2 BLOCKERS WERE DAMAGED DURING INSTALLATION IN SURGERY. THEY WERE REMOVED AND REPLACED WITH ALTERNATIVE SCREWS AND BLOCKERS TO COMPLETE THE PROCEDURE WITHOUT REPORTED PATIENT IMPACTS. THIS IS REPORT 4 OF 14 FOR THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 564944 | TL PEDICLE SCREW DIA. 6,5 LG 35 | JAVA TOP LOADING | HWC | ZIMMER SPINE | NA | H26445A |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |