FDA Adverse Event Injury Summary report: N

TRAPEZOID TIBIAL TRAY SZ 5F/4T

MDR report key: 21315351 · Received February 5, 2025

Report

Report Number
1038671-2025-00675
Event Type
Injury
Date Received
February 5, 2025
Date of Event
September 17, 2021
Report Date
February 5, 2025
Manufacturer
EXACTECH, INC.
Product Code
JWH
UDI-DI
10885862047717
PMA / PMN Number
K933610
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
ME
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

1038671-2023-02888 D10: 1911258 - 200-65-09 - CR TIBIAL INSERT SZ 5, 9MM, SLOPE + 2238408 - 230-02-05 - OPTETRAK ASY,CR CEMENTED FEMORAL, SZ 5 MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 1038671-2023-02888. THE DEVICE WILL NOT BE RETURNED FOR ANALYSIS; HOWEVER, AN INVESTIGATION OF THE REPORTED EVENT IS IN PROGRESS. ONCE THE INVESTIGATION IS COMPLETED, A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED. IF ANY FURTHER INFORMATION IS OBTAINED THAT WOULD CHANGE OR ALTER ANY INFORMATION PROVIDED, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY.

Description of Event or Problem · 0

IT WAS REPORTED THAT APPROXIMATELY 84 MONTHS AFTER A LEFT TOTAL KNEE REPLACEMENT PROCEDURE, THE PATIENT UNDERWENT A REVISION PROCEDURE TO ADDRESS PROSTHESIS WEAR, OSTEOLYSIS AND SCAR TISSUE. INITIAL SURGERY AND REVISION SURGERY OPERATIVE NOTES WERE PROVIDED. PATIENT LEFT THE OPERATING ROOM IN STABLE CONDITION. POST OPERATIVE DIAGNOSIS NOTED WEAR OF THE IMPLANT. NO FURTHER ISSUES OR COMPLICATIONS WERE REPORTED. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
50529 TRAPEZOID TIBIAL TRAY SZ 5F/4T PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL JWH EXACTECH, INC. 10885862047717

Patients

Seq Age Sex Outcome Treatment
1 64 YR Male Hospitalization| R SEE H11.