MAUDE Adverse Event Report: ZIMMER BIOMET, INC. 36MM I.D. SIZE MM ELEVATED RIM LINER USE WITH 60MM O.D. SIZE MM SHELL; PROSTHESIS, HIP

Model Number	N/A
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Failure of Implant (1924); Osteolysis (2377)
Date of Event	06/13/2023
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that there was an initial revision of unknown hip product for unknown reasons with implantation of zimmer biomet product at that time.Subsequently, a second revision was performed approximately a year and a half later due to loosening of the acetabular implant.Osteolysis was found.Attempts have been made and no further information has been provided.
Additional Manufacturer Narrative
(b)(4).D10: cat# 00877503603 lot# 2041128 bioloxâ® delta, ceramic femoral head, l, 㸠36/+3.5, taper.(b)(6) 14.Unk alloclassic stem.Unk g7 shell.Unk g7 screw.G2: foreign: australia.Visual examination of a provided picture identified the ceramic head, liner, and shell explanted and covered in bio-debris.The liner shows some scratches to the outer spherical surface.The inner spherical surface could not be seen on any device.No further evaluation can be made to the provided pictures.Review of the device history records identified no deviations or anomalies during manufacturing related to the reported event.Medical records were provided and reviewed by a health care professional.Review of the available records identified the following: an initial left total hip arthroplasty was performed with a revision occurring due to a loose cup.A second revision occurred due to a loose cup.Radiographs were provided and reviewed by a health care professional.Review of the available records identified the following: radiolucency adjacent to the lateral acetabular cup and along the proximal femoral implant as noted.Relative horizontal orientation of the acetabular cup.Acetabular protrusion.There is extensive osteolysis.A definitive root cause cannot 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.Multiple mdr reports were filed for this event, please see associated reports: 0001822565 - 2023 - 01782.0001822565 - 2023 - 01783.0001822565 - 2023 ¿ 01784.0001822565 - 2023 - 02740.0002648920 - 2023 - 00241.

• Brand Name: 36MM I.D. SIZE MM ELEVATED RIM LINER USE WITH 60MM O.D. SIZE MM SHELL
• Common Device Name: PROSTHESIS, HIP
• 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: 17885014
• Report Number: 0001822565-2023-02740
• Device Sequence Number: 7289530
• Product Code: JDI
• UDI-Device Identifier: 00889024149847
• UDI-Public: (01)00889024149847(17)230531(10)64030524
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K200823
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2022
• Device Explanted Year: 2023
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial
• Report Date (Section B): 10/04/2023

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: 05/31/2023
• Device Model Number: N/A
• Device Catalogue Number: 00875201436
• Device Lot Number: 64030524
• 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: 10/03/2023
• Initial Report FDA Received Date: 10/06/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 06/26/2018
• 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
• 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
• Patient Weight: 94 KG