MAUDE Adverse Event Report: ZIMMER BIOMET, INC. MODULAR HUMERAL HEAD 24 MM HEAD HEIGHT 46 MM SPHERICAL HEAD DIAMETER; SHOULDER PROSTHESIS/EXTREMITIES

Model Number	N/A
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Arthritis (1723); Connective Tissue Disease (1786); Pain (1994); Loss of Range of Motion (2032)
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Multiple mdr reports were filed for this event, please see associated reports: 0001822565-2022-00343.Concomitant medical products: item#: 00430000813, modular humeral stem 8 mm stem diameter 130 mm stem length; lot#: 61689505.Customer has indicated that the product will not be returned to zimmer biomet for investigation, as it remains implanted.The investigation is in process.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 right shoulder arthroplasty, subsequently, the patient has been indicated for a revision due to rotator cuff deficiency and glenohumeral arthritis.
Additional Manufacturer Narrative
(b)(4).Multiple mdr reports were filed for this event, please see associated reports: 0001822565-2022-00343.Concomitant medical products: item#: 00430000813, modular humeral stem 8 mm stem diameter 130 mm stem length; lot#: 61689505.Customer has indicated that the product will not be returned to zimmer biomet for investigation, as it remains implanted.The investigation is in process.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 right shoulder arthroplasty, subsequently, the patient has been indicated for a revision due to rotator cuff deficiency and glenohumeral arthritis.
Additional Manufacturer Narrative
(b)(4).This follow-up report is being to report a correction as the this device was found to be not related/ reportable, because of that the event is being reported on mfr 0001822565-2022-00343-1.No product was returned or pictures provided; visual and dimensional evaluations could not be performed.Review of the device history record(s) identified no deviations or anomalies during manufacturing related to the reported event.Radiographs were provided and reviewed by a health care professional.Review of the available records identified the following: the intramedullary component of the humerus is at least partially cemented with cement mantle most prominent proximally and medially.The intramedullary component is located eccentrically laterally the level of the proximal humeral diaphysis and slightly eccentrically medially at its tip.There is a thin periprosthetic lucency located medial to the cement mantle at the level of the proximal humerus.Also noted periprosthetic lucencies near the tip of the hardware component.The humeral head component is high-riding and located superior with respect to the glenoid, causing narrowing of the subacromial joint space.Besides the periprosthetic lucencies, bone quality appears relatively normal.Root cause for the head was identified as patient condition as rotator cuff deficiency was noted.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.
Event or Problem Description
No further event information available at the time of this report.
Additional Manufacturer Narrative
(b)(4).This follow-up report is being submitted to relay additional/corrected information.Multiple mdr reports were filed for this event, please see associated reports: 0001822565-2022-00343-2.Upon receiving additional information of the reported event, it was determined to be not reportable due to disease progression evidenced by surgeons documentation of rotator cuff failure and patient's clinical signs of pain, and failure impacting patients daily activities and limiting rom.The initial report should be voided.

• Brand Name: MODULAR HUMERAL HEAD 24 MM HEAD HEIGHT 46 MM SPHERICAL HEAD DIAMETER
• Common Device Name: SHOULDER PROSTHESIS/EXTREMITIES
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 56 e. bell drive; warsaw IN 46582
• 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: 13453035
• Report Number: 0001822565-2022-00342
• Device Sequence Number: 5046827
• Product Code: KWT
• UDI-Device Identifier: 00889024264069
• UDI-Public: (01)00889024264069(10)61689505
• Combination Product (Y/N): N
• Initial Reporter State: IL
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other,Health Professional,Distributor
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 06/15/2022

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: 02/28/2021
• Device Model Number: N/A
• Device Catalogue Number: 00430004624
• Device Lot Number: 61689505
• 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: 01/25/2022
• Supplement Date Received by Manufacturer: 04/21/2022; 05/16/2022
• Initial Report FDA Received Date: 02/04/2022
• Supplement Report FDA Received Date: 04/28/2022; 06/15/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 02/23/2011
• 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: Required Intervention; Hospitalization
• Patient Sex: Female