5.0MM SCHANZ SCREW BLUNTED TROCAR POINT 250MM
Report
- Report Number
- 8030965-2022-05023
- Event Type
- Injury
- Date Received
- July 21, 2022
- Date of Event
- May 1, 2022
- Manufacturer
- SYNTHES GMBH
- Product Code
- KTT
- UDI-DI
- 10886982181596
- PMA / PMN Number
- K082650
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CI
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
ADDITIONAL PROCODE: LXT. COMPLAINANT PART IS NOT EXPECTED TO BE RETURNED FOR MANUFACTURER REVIEW/INVESTIGATION. WITHOUT A LOT NUMBER THE DEVICE HISTORY RECORDS REVIEW COULD NOT BE COMPLETED. PRODUCT WAS NOT RETURNED. BASED ON THE INFORMATION AVAILABLE, IT HAS BEEN DETERMINED THAT NO CORRECTIVE AND/OR PREVENTATIVE ACTION IS PROPOSED. THIS COMPLAINT WILL BE ACCOUNTED FOR AND MONITORED VIA POST MARKET SURVEILLANCE ACTIVITIES. IF ADDITIONAL INFORMATION IS MADE AVAILABLE, THE INVESTIGATION WILL BE UPDATED AS APPLICABLE. DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.
DEVICE REPORT FROM CHILE REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT ON (B)(6) 2022 THE PATIENT WAS ADMITTED TO THE ICU OF THE HOSPITAL, WITH FOUR BROKEN SCHANZ SCREWS. THE PATIENT WAS ADMITTED IN A STATE OF COMPROMISED CONSCIOUSNESS, THERE IS NO FURTHER INFORMATION AVAILABLE. THIS REPORT IS FOR A 5.0MM SCHANZ SCREW BLUNTED TROCAR POINT 250MM. THIS IS REPORT 3 OF 4 FOR PC-(B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1719838 | 5.0MM SCHANZ SCREW BLUNTED TROCAR POINT 250MM | APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT | KTT | SYNTHES GMBH | 294.57 | 10886982181596 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown | Required Intervention | SCHANZSCR Ø5 L250/50 SST| SCHANZSCR Ø5 L250/50 SST| SCHANZSCR Ø5 L250/50 SST |