MAUDE Adverse Event Report: ZIMMER BIOMET, INC. 32MM I.D. SIZE HH NEUTRAL LINER USE WITH 50MM O.D. SIZE HH SHELL; PROSTHESIS, HIP

Model Number	N/A
Medical Device Problem Code	Device Dislodged or Dislocated (2923)
Health Effect - Clinical Code	Joint Dislocation (2374)
Date of Event	11/20/2023
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Multiple mdr reports were filed for this event, please see associated reports: 0001822565 - 2023 - 03530, 0001822565 - 2023 - 03532.D10: cat# 00811400110 lot# unk femoral stem 12/14 neck taper ext.Offset size 1 130 mm stem length.G2: foreign: united kingdom.The customer has indicated that the product is in process of being returned to zimmer biomet for investigation.Once the investigation has been completed, a follow-up mdr will be submitted.
Event or Problem Description
It was reported that the patient underwent a total hip replacement.Subsequently, the patient had a fall, landing on the hip that was replaced, causing the dislocation.The patient underwent a revision procedure approximately 1 month post implantation.Perioperatively, the surgeon decided to exchange the shell due to shell malposition and the liner for an elevated liner.On removal of the femoral head, the stem was removed and exchanged for the same offset and size.It was reported that no further information is available.
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.Lot identification is necessary for review of device history records, lot identification was not provided.Medical records were not provided.It is unknown if the shell was placed incorrectly, or was placed that way dependent on patient anatomy.While the cup position could be a contributing factor to the dislocation, a definitive root cause cannot be identified.Additionally, the reason for the fall is unknown.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 information at the time of this report.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.The following sections were {update/corrected}.Updated: d4; d9; g3; h2.
Event or Problem Description
No further information at the time of this report.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.The following sections were {update/corrected}.Updated: d4; d5; g3; h2; h3; h4; h6: h10.Visual examination of the returned product identified liner was returned seated in the shell.Shell has bio debris embedded in the outer spherical surface.Shell rim face is discolored, gouged, and indented.Liner shows one anti rotation scallop missing, screw hole, and gouges in the spherical surface.Liner has rim wear consistent to the reported dislocation.No other damage was noted.Review of the device history records identified no deviations or anomalies during manufacturing related to the reported event.Root cause unchanged.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 information at the time of this report.

• Brand Name: 32MM I.D. SIZE HH NEUTRAL LINER USE WITH 50MM O.D. SIZE HH 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: 18317686
• Report Number: 0001822565-2023-03531
• Device Sequence Number: 6152171
• Product Code: JDI
• UDI-Device Identifier: 00889024149106
• UDI-Public: (01)00889024149106(17)280310(10)65843426
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• PMA/510(K) Number: K200823
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2023
• Device Explanted Year: 2023
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 09/09/2025

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?: Yes
• Operator of Device: Lay User/Patient
• Device Model Number: N/A
• Device Catalogue Number: 00875100932
• Device Lot Number: 65843426
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• 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: 11/20/2023
• Supplement Date Received by Manufacturer: 03/25/2024; 03/20/2025; 09/04/2025
• Initial Report FDA Received Date: 12/13/2023
• Supplement Report FDA Received Date: 03/28/2024; 04/01/2025; 09/09/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 03/12/2023
• 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: Hospitalization; Required Intervention
• Patient Sex: Unknown