MAUDE Adverse Event Report: ENCORE MEDICAL L.P. TURON SHOULDER; TURON PEGGED GLENOID IMPLANT, SIZE 50

Model Number	520-01-250
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	06/03/2019
Type of Reportable Event	Serious Injury
Event or Problem Description
Revision surgery - due to glenoid loosening.
Additional Manufacturer Narrative
Manufacturer narrative: the reason for this revision surgery was reported as loosening.The previous surgery and the surgery detailed in this event occurred 7.3 years apart.The healthcare professional indicated there was no delay in surgery and another suitable device was available for use.The revision surgery was completed as intended.The device was disposed of at hospital and not made available to djo surgical for examination.A review of the device history records (dhr) show that the reported components used in the previous surgery, when released for use, met design and manufacturing requirements.There were no non-conforming material reports (ncmr) associated with the products that may have contributed to the reported event.The devices were verified to have gone through an acceptable sterilization process and were within its expiration date at the time of the previous surgery.Customer complaint history of the reported devices showed no present trends or on-going issues that are needing a review.The root cause of this complaint was a revision surgery due to loosening.There were no findings during this evaluation that indicate the reported devices were defective.No information was submitted with the complaint regarding pre-existing conditions of the patient or any activities the patient was involved in that may have contributed to the event.There are multiple factors that may contribute to an event that are outside the control of djo surgical.There are no indications of a product or process issue affecting implant safety or effectiveness.

• Brand Name: TURON SHOULDER
• Common Device Name: TURON PEGGED GLENOID IMPLANT, SIZE 50
• Manufacturer (Section D): ENCORE MEDICAL L.P.; 9800 metric blvd; austin, tx 78758-5445, TX 78758 5445
• MDR Report Key: 8759991
• Report Number: 1644408-2019-00616
• Device Sequence Number: 16785511
• Product Code: KWS
• UDI-Device Identifier: 00888912024976
• UDI-Public: (01)00888912024976
• Combination Product (Y/N): N
• Initial Reporter State: MN
• Initial Reporter Country: US
• PMA/510(K) Number: K123982
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2012
• Device Explanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 02/20/2020

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: 07/31/2016
• Device Model Number: 520-01-250
• Device Catalogue Number: 520-01-250
• Device Lot Number: 193G1019
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 06/03/2019
• Supplement Date Received by Manufacturer: 01/24/2020
• Initial Report FDA Received Date: 07/03/2019
• Supplement Report FDA Received Date: 02/22/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 520-00-000 LOT 878C1075; 520-00-000. LOT UNKNOWN.; 520-01-010 LOT 455G1033; 520-01-010. LOT UNKNOWN.; 520-50-018 LOT 929C1003; 520-50-018. LOT UNKNOWN.; 520-00-000. LOT UNKNOWN.; 520-01-010. LOT UNKNOWN.; 520-50-018. LOT UNKNOWN.
• Outcome Attributed to Adverse Event: Required Intervention