MAUDE Adverse Event Report: ZIMMER BIOMET, INC. LINER HIGH WALL 40 MM; PROSTHESIS, HIP

Model Number	N/A
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	01/15/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Concomitant medical devices: 110010271 ¿ g7 multihole shell - r3713970a; 11-300817 ¿ arcos distal stem ¿ 838140; 11-301323 ¿ arcos cone - 213330; 650-1067 ¿ biolox delta taper 3031101; 650-1058 ¿ biolox delta head ¿ 2993794; 00625006520 - bone screw - 63187339; 00625006540 ¿ bone screw ¿ 63604707; 00625006540 ¿ bone screw ¿ 64202377; 00625006515 ¿ bone screw - 629035991.Customer has indicated that the product will not be returning for the investigation as the product location is unknown.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 event, please see associated reports: 0001822565 - 2021 - 00623, 0001822565 - 2021 - 00625, 0001822565 - 2021 - 00626, 0001822565 - 2021 - 00627.
Event or Problem Description
It was reported that patient underwent a first stage revision after an unknown amount of time post implantation, a second stage revision approximately 2 months later and 3 more surgeries within a 15 month period of time.Subsequently, the patient underwent another revision approximately 1 month after the last due to infection.Attempts have been made and additional information on the reported event is unavailable at this time.
Event or Problem Description
The received additional information does not change the final conclusions of previous investigation.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.It was reported that multiple right hip revision have been performed since on (b)(6) 2019, with a known history of prior right hip infection.With multiple surgical revision to right hip, increases the patients risk to develop infections.During the investigation process a review of the sterile certifications were reviewed and found to be conforming with no applicable deviations.Devices were verified to have gone through acceptable sterilization process following iso/aami/astm & eu published guidelines.There are multiple factors that may contribute to an infection that are outside the control of zimmer biomet, such as external factors, i.E.Hospital/surgical environment, provider related risk factors, and/or patient comorbidities/risk factors.As there are no indications of a product or process issues identified affecting implant safety or effectiveness, therefore implanted products are not identified as the source or contributing to the reported infection.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.

• Brand Name: LINER HIGH WALL 40 MM
• Common Device Name: PROSTHESIS, HIP
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 56 e. bell drive; warsaw IN 46582
• MDR Report Key: 11444331
• Report Number: 0001822565-2021-00622
• Device Sequence Number: 4014401
• Product Code: LPH
• UDI-Device Identifier: 00889024520578
• UDI-Public: (01)00889024520578(17)250331(10)64714864
• Combination Product (Y/N): N
• Initial Reporter State: IN
• Initial Reporter Country: US
• PMA/510(K) Number: K190660
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Device Explanted Year: 2021
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: distributor,health profession
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 06/10/2021

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: 03/31/2025
• Device Model Number: N/A
• Device Catalogue Number: 30124009
• Device Lot Number: 64714864
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 02/12/2021
• Supplement Date Received by Manufacturer: 06/09/2021
• Initial Report FDA Received Date: 03/09/2021
• Supplement Report FDA Received Date: 06/10/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• 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: Hospitalization; Required Intervention
• Patient Age: 45 YR