MAUDE Adverse Event Report: ZIMMER BIOMET, INC. VIT E LINER ELEVATED KK 36; PROSTHESIS, HIP

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	03/21/2022
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the patient was revised due to pain and poor cup position approximately 2 years post implantation.Attempts have been made and additional information on the reported event is unavailable.
Additional Manufacturer Narrative
(b)(4).Catalog number:00-8757-056-01, lot number:77010387 brand name: continuum tm shell.Catalog number:00-8852-012-36, lot number: 64802356 brand name: vit e liner elevated.Catalog number:00-7848-022-00, lot number:64746102 brand name: kinectiv modular.Catalog number:00-6250-065-30, lot number:j6793110 brand name: bone screw.Catalog number:00-6250-065-36, lot number:j6828155 brand name: bone screw.Catalog number: 00-7713-011-00, lot number:64816986 brand name: m/l taper stem.Catalog number: 00-8775-036-02, lot number:3043607 brand name: biolox delta head.Multiple reports were submitted along with this report: 0001822565-2022-01023 and 0001822565-2022-01025.Customer has indicated that the product will not be returned to zimmer biomet for investigation.The investigation is in process.Once theinvestigation has been completed, a follow-up mdr will be submitted.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.Radiographs were provided and reviewed by a health care professional.Review of the available records identified the following: slight decreased lateral inclination of the left acetabular cup.Reported event was confirmed by review of x-rays provided.Review of the device history records identified no deviations or anomalies during manufacturing related to the reported event.Root cause could not be determined.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: VIT E LINER ELEVATED KK 36
• Common Device Name: PROSTHESIS, HIP
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 56 e. bell drive; warsaw IN 46582
• Manufacturer (Section G): ZIMMER BIOMET, INC.; 56 e. bell drive; warsaw IN 46582
• Manufacturer Contact: christina arnt ; 56 e. bell dr.; warsaw, IN 46582 ; 5745273773
• MDR Report Key: 14117314
• Report Number: 0001822565-2022-01024
• Device Sequence Number: 4334498
• Product Code: OQG
• UDI-Device Identifier: 00889024155589
• UDI-Public: (01)00889024155589(17)210925(10)64802356
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K120370
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 05/20/2022

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: 09/21/2025
• Device Model Number: N/A
• Device Catalogue Number: 00885201236
• Device Lot Number: 64802356
• 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: 03/23/2022
• Supplement Date Received by Manufacturer: 05/09/2022
• Initial Report FDA Received Date: 04/15/2022
• Supplement Report FDA Received Date: 05/20/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 10/21/2020
• 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
• Concomitant Medical Products and Therapy/Usage Dates: SEE H10 NARRATIVE.
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Sex: Female