MAUDE Adverse Event Report: EXACTECH, INC. LOGIC TIB INSERT IMPL CRC, SZ 5, 9MM; PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL

Catalog Number	02-012-51-5009
Medical Device Problem Code	Naturally Worn (2988)
Health Effect - Clinical Codes	Cyst(s) (1800); Bone Fracture(s) (1870); Failure of Implant (1924); Unspecified Infection (1930); Pain (1994); Synovitis (2094); Osteolysis (2377); Swelling/ Edema (4577)
Date of Event	05/31/2023
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Section h10: (h3) pending evaluation: (d10) concomitant device(s): 4009299; 02-010-04-0350 - logic cr femoral por, right, sz 5.3659553; 02-012-45-5060 - lgc tibial fit tray cem sz 5f / 6t.4698645; 200-02-38 - three peg patella 38mm.11045016039; a10012 - gps implant kit v2.
Event or Problem Description
As reported, approximately 6 years post op initial right tka, this 75 y/o female patient was revised due to poly wear.Everything was removed and used other company¿s products.No product details available.Patient was last known to be in stable condition following the event.No other patient information/medical history reported.Product not returning - disposed at the hospital.
Additional Manufacturer Narrative
Section h10: (h3) the revision reported may have been the result of a combination of prosthesis wear, patient-related conditions, and/or inclusion of the implanted tibial insert in the packaging recall.However, this cannot be confirmed as devices were not available for evaluation.Section h11: *the following sections have corrected information: (h6) component code: 734, bearings.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional and corrected information.The following sections were updated: b5, g1 contact first/last name.The following sections were corrected: h6 clinical code.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.
Event or Problem Description
As reported, approximately 6 years post op initial right tka, this 75 y/o female patient was revised due to poly wear.Recently reported were the following for this patient: massive osteolysis proximal lateral tibia, large lytic lesion in proximal tibia, pathological fracture proximal tibia, lateral collateral ligament incompetent, osteoarthritis, pain and swelling, antalgic gait, cysts, tibial loosening, infection.All components were removed and used competitor's products.Patient was last known to be in stable condition following the event.No other patient information/medical history reported.
Additional Manufacturer Narrative
"this follow-up report is being submitted to relay additional and/or corrected information.The following sections were corrected: b1, b2, g2, h6.The revision reported may have been the result of a combination of prosthesis wear, tibial loosening, patient-related conditions, and/or the inclusion of the polyethylene in the packaging recall.However, this cannot be confirmed as the devices were not available for evaluation and no radiographs or relevant clinical information was provided.If any further information is obtained that would change or alter any information provided, a supplemental report will be filed accordingly.".

• Brand Name: LOGIC TIB INSERT IMPL CRC, SZ 5, 9MM
• Common Device Name: PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL
• Manufacturer (Section D): EXACTECH, INC.; 2320 nw 66 court; gainesville FL 32653
• Manufacturer (Section G): EXACTECH, INC.; 2320 nw 66 ct; gainesville FL 32653
• Manufacturer Contact: geoff gannon ; 3523771140
• MDR Report Key: 17180573
• Report Number: 1038671-2023-01434
• Device Sequence Number: 15050870
• Product Code: JWH
• UDI-Device Identifier: 10885862230560
• UDI-Public: 10885862230560
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K123342
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2023
• Reporter Type: Manufacturer
• Report Source: Foreign,Consumer,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 05/13/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 10/27/2023
• Device Catalogue Number: 02-012-51-5009
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/02/2023
• Supplement Date Received by Manufacturer: 08/10/2023; 03/18/2024; 05/07/2025
• Initial Report FDA Received Date: 06/22/2023
• Supplement Report FDA Received Date: 08/29/2023; 12/21/2024; 05/13/2025
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 10/28/2015
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: SEE H10.
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 75 YR
• Patient Sex: Female