FDA Adverse Event Injury Summary report: N

LOGIC CR TIB INSERT SLOPE++, SZ 3, 11MM

MDR report key: 19643542 · Received July 1, 2024

Report

Report Number
1038671-2024-02218
Event Type
Injury
Date Received
July 1, 2024
Date of Event
March 14, 2023
Report Date
July 1, 2024
Manufacturer
EXACTECH, INC.
Product Code
JWH
UDI-DI
10885862174420
PMA / PMN Number
K111400
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

D10: CONCOMITANT DEVICES: 3891609 02-010-03-0230 - LOGIC CR FEMORAL CEM, LEFT, SZ 3 4134237 02-012-45-3030 - LGC TIBIAL FIT TRAY CEM SZ 3F / 3T 4162281 200-02-29 - THREE PEG PATELLA 29MM THE PRODUCT ASSOCIATED WITH THE REPORTED EVENT IS WITHIN THE SCOPE OF RECALL Z-0021-2022; HOWEVER, THERE IS INSUFFICIENT INFORMATION TO EVALUATE WHETHER THE SUBJECT ISSUE OF THE RECALL WAS A CAUSE OR CONTRIBUTOR TO THE REPORTED EVENT. THE DEVICE WAS NOT RETURNED FOR EVALUATION AND NO MEDICAL OR OTHER RECORDS CONTAINING TREATMENT INFORMATION OR PATIENT INFORMATION HAVE BEEN RECEIVED; THEREFORE, THE REPORTED EVENT CANNOT BE CONFIRMED, NOR CAN THE CIRCUMSTANCES OR POTENTIAL CAUSES OR CONTRIBUTORS TO THE ALLEGED EVENT BE EVALUATED. SHOULD ADDITIONAL, MATERIAL INFORMATION BECOME AVAILABLE THAT PERMITS MORE ANALYSIS OR CONCLUSIONS, A SUPPLEMENTAL REPORT WILL BE FILED ACCORDINGLY.

Description of Event or Problem · 0

IT WAS REPORTED VIA LEGAL DOCUMENTATION THAT APPROXIMATELY 88 MONTHS AFTER A LEFT TOTAL KNEE REPLACEMENT PROCEDURE, THE PATIENT UNDERWENT A REVISION PROCEDURE TO ADDRESS PROSTHESIS WEAR. NO FURTHER ISSUES OR COMPLICATIONS WERE REPORTED. NO ADDITIONAL INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1270914 LOGIC CR TIB INSERT SLOPE++, SZ 3, 11MM PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL JWH EXACTECH, INC. 10885862174420

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Hospitalization| R SEE H11