MAUDE Adverse Event Report: ZIMMER BIOMET, INC. SHELL WITH MULTI HOLES POROUS 58 MM O.D. SIZE LL FOR USE WITH LL LINERS; PROSTHESIS, HIP

Model Number	N/A
Medical Device Problem Code	Migration (4003)
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	11/22/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Brand name: item number 00875201332 item name liner elevated rim 32 mm i.D.Size ll for use with 58 mm o.D.Size ll shell lot # 64360460.Report source: (b)(6).The device will not be returned for analysis as it was discarded; however, an investigation of the reported event is in progress.Once the investigation is completed, a supplemental mdr will be submitted.Multiple mdr reports were filed for this event, please see associated reports:  0002648920-2021-00443, 0002648920-2021-00442, 0002648920-2021-00441, 0002648920-2021-00440, 0002648920-2021-00439, 0002648920-2021-00438, 0002648920-2021-00437, 0002648920-2021-00436.
Event or Problem Description
It was reported that patient underwent initial hip arthroplasty.Subsequently, patient was revised 2 years post implantation for aseptic loosening.Continuum cup explanted and replaced with a cup from another company.Attempts have been made and additional information on the reported event is unavailable at this time.
Event or Problem Description
No additional event information to report at this time.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.Corrected: e1 (country).G2: report source new zealand.Radiographs were provided and reviewed an hcp.The review notes the right total hip arthroplasty with possible evidence of metallosis.Suggestion of loosening of the acetabular cup is also noted.Visual examination of the provided pictured identified the shell was explanted and covered in bio debris.No further evaluation can be made from provided photos.Dhr was reviewed and no discrepancies were found.The root cause is unable to 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.

• Brand Name: SHELL WITH MULTI HOLES POROUS 58 MM O.D. SIZE LL FOR USE WITH LL LINERS
• 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: 12960855
• Report Number: 0001822565-2021-03502
• Device Sequence Number: 17498806
• Product Code: JDI
• UDI-Device Identifier: 00889024151475
• UDI-Public: (01)00889024151475(17)290630(10)64311163
• Combination Product (Y/N): N
• Initial Reporter Country: NZ
• PMA/510(K) Number: K200823
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Device Explanted Year: 2021
• 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
• Report Date (Section B): 02/21/2022

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?: Yes
• Operator of Device: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: 00875705802
• Device Lot Number: 64311163
• 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: 11/22/2021
• Supplement Date Received by Manufacturer: 02/17/2022
• Initial Report FDA Received Date: 12/08/2021
• Supplement Report FDA Received Date: 02/23/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 06/01/2019
• 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: 79 KG