MAUDE Adverse Event Report: ZIMMER BIOMET, INC. VGD VE PS TIB BRG 71/75X12MM; PROSTHESIS, KNEE

Model Number	N/A
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Pain (1994)
Date of Event	12/20/2022
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Medical devices: 183108 - van ps open intl fem-rt 65 - j6865010, 141233 - biomet cc cruciate tray 71mm - j7018320, 184784 - series a pat thn 31 3 peg - 191070, 183099 - vanguard fem pegs set 2 - 624660.Customer has indicated that the product will not be returned to zimmer biomet for investigation.Once the investigation has been completed, a follow-up mdr will be submitted.Multiple mdr reports were filed for this event, please see associated reports: 0001825034-2022-02331, 0001825034-2022-02332, 0001825034-2022-02336, 0001825034-2022-02337.
Event or Problem Description
It was reported that the patient underwent a total knee replacement approximately one year ago due to pain.The patient alleges that the operating physician stated that the patient's implant had shifted and the patient reported having a similar pain from their leg to their ankle and down their leg as they did prior to the surgery.The patient further alleged that their new surgeon advised that the implant was too large and would need to be revised.The patient is scheduled for a revision surgery; however, no revision procedure has been reported to date.Attempts have been made and no further information has been provided.
Event or Problem Description
It was further reported that the patient underwent a revision knee surgery approximately 14 months post-implantation.Attempts have been made and no further information has been provided.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.No product was returned or pictures provided; visual and dimensional evaluations could not be performed.The device history record was reviewed and no discrepancies relevant to the reported event were found.Medical records were not provided.A definitive root cause cannot be determined.If any further information is found which would change or alter any conclusions or information, a supplemental report 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: VGD VE PS TIB BRG 71/75X12MM
• Common Device Name: PROSTHESIS, KNEE
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 56 e. bell drive; p.o. box 587; warsaw IN 46581
• Manufacturer (Section G): ZIMMER BIOMET, INC.; 56 e. bell drive; p.o. box 587; warsaw IN 46581
• Manufacturer Contact: jennifer rapsavage ; 56 e. bell dr.; warsaw, IN 46582 ; 5745260384
• MDR Report Key: 15635499
• Report Number: 0001825034-2022-02334
• Device Sequence Number: 5810587
• Product Code: JWH
• UDI-Device Identifier: 00889024565685
• UDI-Public: (01)00889024565685(17)260310(10)65022128
• Combination Product (Y/N): N
• Initial Reporter State: NC
• Initial Reporter Country: US
• PMA/510(K) Number: K183583
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Consumer,Distributor
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 03/06/2023

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 Expiration Date: 03/10/2026
• Device Model Number: N/A
• Device Catalogue Number: VE183642
• Device Lot Number: 65022128
• 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: 09/30/2022
• Supplement Date Received by Manufacturer: 01/11/2023; 03/02/2023
• Initial Report FDA Received Date: 10/19/2022
• Supplement Report FDA Received Date: 01/24/2023; 03/07/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 04/05/2021
• 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
• Concomitant Medical Products and Therapy/Usage Dates: SEE H10.
• Outcome Attributed to Adverse Event: Other
• Patient Age: 64 YR
• Patient Sex: Female