MAUDE Adverse Event Report: ZIMMER BIOMET, INC. M2A-MAGNUM 42-50 TPR INSRT STD; PROSTHESIS, HIP

Model Number	N/A
Medical Device Problem Code	Corroded (1131)
Health Effect - Clinical Codes	Host-Tissue Reaction (1297); Pain (1994); Tissue Damage (2104); Metal Related Pathology (4530)
Date of Event	02/13/2017
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).Concomitant medical products: catalog number: 157444, lot number: 528290, brand name: m2a-magnum head; catalog number: us157850, lot number: 702560, brand name: m2a magnum cup; catalog number: 11-103206, lot number: 853440, brand name: taperloc stem; catalog number: 139256, lot number:760510, brand name: m2a magnum taper insert.Multiple mdr reports were filed for this event, please see associated reports: 0001825034-2016-04021, 0001825034-2019-02858, 0001825034-2017-06059.The patient underwent a revision procedure due to failed hip replacement.Patient had abnormal cobalt chromium levels and pain.Metallosis with wear debris, trunnionis, and abductor muscle tear were identified during the procedure.Mild discoloration was observed on the trunnion.The acetabulum was stable without evidence of failure.The femoral head was replaced with ceramic head and e poly mobile bearing system.Patient tolerated the procedure well.Reported event was confirmed by review of medical records provided.Received additional information does not change the final conclusions of previous investigation.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.Device not returned for evaluation.
Event or Problem Description
The patient underwent a revision procedure due to failed hip replacement.Patient had abnormal cobalt chromium levels and pain.Metallosis with wear debris, trunnionis, and abductor muscle tear were identified during the procedure.Mild discoloration was observed on the trunnion.The acetabulum was stable without evidence of failure.The femoral head was replaced with ceramic head and e poly mobile bearing system.Patient tolerated the procedure well.
Event or Problem Description
No further event information available at the time of this report.
Additional Manufacturer Narrative
This follow-up report is being submitted to relay additional information.One m2a-magnum mod hd sz 44mm and one m2a-magnum 42-50 tpr insrt std were returned and evaluated.Upon visual inspection the insert was installed in the head with the od of the head having a wear line.There is no visible debris inside of the taper.Review of device history records found these units were released to distribution with no deviations or abnormalities.Root cause could not be determined with information available.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: M2A-MAGNUM 42-50 TPR INSRT STD
• 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: 8752834
• Report Number: 0001825034-2019-02859
• Device Sequence Number: 19417836
• Product Code: KWA
• UDI-Device Identifier: 00880304428058
• UDI-Public: (01)00880304428058(17)280522(10)760510
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• PMA/510(K) Number: K042037
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2014
• Device Explanted Year: 2017
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Consumer,Health Professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 05/12/2022

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 Expiration Date: 05/28/2022
• Device Model Number: N/A
• Device Catalogue Number: 139256
• Device Lot Number: 760510
• 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: 06/25/2019
• Supplement Date Received by Manufacturer: 04/27/2022
• Initial Report FDA Received Date: 07/02/2019
• Supplement Report FDA Received Date: 05/12/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 05/05/2012
• 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