MAUDE Adverse Event Report: ZIMMER BIOMET, INC. PERSONA REVISION CEMENTED STANDARD FEMORAL COMPONENT LEFT SIZE 7; PROSTHESIS, KNEE

Model Number	N/A
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Pain (1994); Loss of Range of Motion (2032); Synovitis (2094); Swelling/ Edema (4577); Joint effusion (4849)
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the patient underwent an aspiration, arthrocentesis and triamcinolone acetonide injections to address pain, synovitis, loss of range of motion, joint effusion and swelling approximately six months following left knee arthroplasty.Initial operative notes noted no intraoperative complications.
Additional Manufacturer Narrative
Cmp-0926319 d10 - concomitant devices - persona revision straight splined uncemented stem extension 14mm x +135mm catalog #: 42560113514 lot #: 64847681, persona revision cemented tibial component left size g catalog #: 42542007901 lot #: 64817981, persona revision offset splined uncemented stem extension 3mm x 10mm x +135mm catalog #: 42560313510 lot #: 64783515, persona posterior stabilized fixed bearing articular surface left 13mm catalog #: 42512400913 lot #: 64355165, biomet bone cement r 1x40 us catalog #: 110035368 lot #: ay09ac0107.The complainant has indicated that the product will not be returned to zimmer biomet for investigation, as the device remains implanted.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.Multiple mdr reports were filed for this patient; please see all reports associated with this event: 0001822565-2024-00866, 0001822565-2024-00867, 0001822565-2024-00868, 3007963827-2024-00069 h3 other text : investigation incomplete.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.The following sections were updated: b4, g3, g6, h2, h3, h6, h11.The following sections were corrected: h4 h6 - component code - proposed code is mechanical (04) femur medical records were received and findings previously reported.The device history records were reviewed and no discrepancies were identified.A definitive root cause could not be determined with the information provided.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.
Event or Problem Description
No further event information available at the time of this report.

• Brand Name: PERSONA REVISION CEMENTED STANDARD FEMORAL COMPONENT LEFT SIZE 7
• 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: 18901924
• Report Number: 0001822565-2024-00865
• Device Sequence Number: 15425557
• Product Code: JWH
• UDI-Device Identifier: 00889024562554
• UDI-Public: (01)00889024562554(17)301120(10)64890357
• Combination Product (Y/N): N
• Initial Reporter State: IN
• Initial Reporter Country: US
• PMA/510(K) Number: K191625
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Study,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 08/07/2024

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: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: 42504606201
• Device Lot Number: 64890357
• 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: 02/20/2024
• Supplement Date Received by Manufacturer: 07/31/2024
• Initial Report FDA Received Date: 03/14/2024
• Supplement Report FDA Received Date: 08/07/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/22/2020
• 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
• If action reported to FDA under 21 USC 360i(g), list FDA-assigned Recall Number or include a statement: N/A
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Male
• Patient Weight: 82 KG
• Patient Ethnicity: Non Hispanic
• Patient Race: White