FDA Adverse Event
Injury
Summary report: N
GMK-HINGE FIXED TIBIAL INSERT SIZE 3/20MM
MDR report key: 19836852
·
Received July 26, 2024
Report
- Report Number
- 3005180920-2024-00546
- Event Type
- Injury
- Date Received
- July 26, 2024
- Date of Event
- June 26, 2024
- Report Date
- July 26, 2024
- Manufacturer
- MEDACTA INTERNATIONAL SA
- Product Code
- KRO
- UDI-DI
- 07630030825156
- PMA / PMN Number
- K130299
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MO, US
- Reporter Occupation
- 003
Narratives
Additional Manufacturer Narrative · 0
BATCH REVIEW PERFORMED ON 02-JUL-2024. LOT 2246199: (B)(4) ITEMS MANUFACTURED AND RELEASED ON 09-MAR-2023. EXPIRATION DATE: 2028-02-20. NO ANOMALIES FOUND RELATED TO THE PROBLEM. TO DATE, (B)(4) ITEMS OF THE SAME LOT HAVE BEEN SOLD WITH NO SIMILAR REPORTED EVENT DURING THE PERIOD OF REVIEW.
Description of Event or Problem · 0
AT ABOUT 1 MONTH AFTER PRIMARY, THE PATIENT CAME IN DUE TO SIGNS OF AN INFECTION AND THE PATHOGEN IS UNKNOWN. THE SURGEON PERFORMED A WASHOUT AND REVISED THE LINER. THE SURGERY WAS COMPLETED SUCCESSFULLY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1776934 | GMK-HINGE FIXED TIBIAL INSERT SIZE 3/20MM | KNEE TIBIAL INSERT | KRO | MEDACTA INTERNATIONAL SA | 2246199 | 07630030825156 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 68 YR | Female | Required Intervention |