MAUDE Adverse Event Report: ZIMMER BIOMET, INC. PERSONA TIBIA TRABECULAR METAL TWO-PEG POROUS FIXED LEFT SIZE F; PROSTHESIS, KNEE

Catalog Number	42530007501
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Pain (1994); Tendinopathy (4887); Crepitus (4893)
Date of Event	01/30/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).D10: medical product: unknown persona femoral component: catalog#ni, lot#ni; unknown persona articular surface: catalog#ni, lot#ni.G2: literature: c.Nakasone, i.Weber, c.Israelite et al., (2025).Early radiographic evaluation of an anatomic porous tantalum tibia: a prospective, multi-center, non-randomized clinical study.The knee (53), 264-272.Https://doi.Org/10.1016/j.Knee.2025.01.010.The product will not be returned to zimmer biomet for investigation, as the product currently remains implanted.The investigation is in process.Upon completion of the investigation, a follow-up mdr be submitted.
Event or Problem Description
On 09-jun-2025, a journal article was retrieved from the knee (2025) that reported a prospective, non-randomized, multi-center study from the usa.The purpose of the study was to investigate the early radiographic, survival and clinical outcomes of a cementless tantalum metal tibial implant with a modular anatomic component.The study reviewed 148 implants, from seven research sites, between 2018 and 2020.A cementless persona trabecular metal tibia was implanted in all patients without the use of autograft bone paste slurry.With regard to the tibial component, 79 patients received a medial congruent vivacit-e component, 25 patients received a posterior stabilized polyethylene component, 25 patients received a posterior stabilized vivacit-e component, and 19 patients received an ultra-congruent vivacit-e component.The patella was resurfaced in 92 knees.The indication for surgery was arthritis, avascular necrosis of the femoral condyle, post-traumatic loss of joint configuration, moderate deformity, and/or the salvage of previously failed surgical attempts that did not include partial or full arthroplasty of the ipsilateral knee.The study population had a mean age of 63.3 years at time of surgery; 84 males/64 females.Follow-up radiographs were conducted at immediate post-operative, six weeks, six months, one year, and two years post-operative.It was reported that one patient experienced it band syndrome/snapping with right knee pain and underwent an intra-articular cortisone injection.Due diligence is in progress for this event; to date no additional information has been provided.
Event or Problem Description
There is no update to the prior event description provided.
Additional Manufacturer Narrative
(b)(4).This follow-up report is being submitted to relay additional and corrected information.The following sections were updated: b4, b5, g3, g6, h2, h6, h10, h11.Corrected data: h6 component code.The product has not been returned.No product evaluation could be performed.The reported event is not related to the device; therefore, a review of the device history records and compatibility is not applicable.The root cause of the reported event is not device related.The iliotibial band is a multiple joint structure that originates at the tuberculum tubercle of the iliac crest and inserts at the anterolateral (gerdy) tubercle of the lateral condyle of the tibia.During a total knee procedure, the iliotibial band is pulled in excess laterally for a prolonged period to allow implantation of the devices.The pulling on the band leads to tissue lengthening and increased inflammation of the iliotibial band while maintaining integrity of the ligament.As the iliotibial band heals, the fibers can become fibrotic leading to painful scar tissue at the distal iliotibial band at the knee.Conservative treatment options for a tight it band includes physical therapy and site-specific mobilization and stretching.If a more invasive approach is required, surgery to release the iliotibial band tightness would occur.This signifies a procedure-related postop complication.If any further information is found that would change or alter any conclusions or information, a supplemental report will be filed accordingly.Zimmer biomet will continue to monitor for trends.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.The following sections have been updated: b3; b4; b5; d1; d2; d4; d6a; d10; g3; g4; h2; h4; h11.D10: medical product: femur cemented cruciate retaining (cr) standard right size 9: catalog#42502606602, lot#64101657; articular surface medial congruent (mc) right 12 mm height use with tibia sizes e-f/cr femur sizes 8-11: catalog#42522100812, lot#63841791; all poly patella cemented 35 mm diameter: catalog#42540000035, lot#64239740.The investigation is in progress.Upon completion of the investigation, a follow-up mdr will be submitted.
Event or Problem Description
No further event information at time of this report.

• Brand Name: PERSONA TIBIA TRABECULAR METAL TWO-PEG POROUS FIXED LEFT SIZE F
• Common Device Name: PROSTHESIS, KNEE
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 1800 w. center st.; warsaw IN 46580
• Manufacturer (Section G): ZIMMER BIOMET, INC.; 1800 w. center st.; warsaw IN 46580
• Manufacturer Contact: jennifer rapsavage ; 56 e. bell dr.; warsaw, IN 46582 ; 5745260384
• MDR Report Key: 22461864
• Report Number: 0001822565-2025-02438
• Device Sequence Number: 18349634
• Product Code: MBH
• UDI-Device Identifier: 00889024246546
• UDI-Public: (01)00889024246546(17)280331(10)62917433
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• PMA/510(K) Number: K173417
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2018
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Study,Literature,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 09/05/2025

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?: No
• Operator of Device: Lay User/Patient
• Device Catalogue Number: 42530007501
• Device Lot Number: 62917433
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/09/2025
• Supplement Date Received by Manufacturer: 07/11/2025; 08/14/2025
• Initial Report FDA Received Date: 07/09/2025
• Supplement Report FDA Received Date: 08/08/2025; 09/08/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 03/22/2018
• 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 H11 NARRATIVE.; SEE H11 NARRATIVE.
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown