MAUDE Adverse Event Report: ENCORE MEDICAL L.P. TURON SHOULDER; TURON PEGGED GLENOID IMPLANT, SIZE 42

Model Number	520-00-000
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	11/27/2018
Type of Reportable Event	Serious Injury
Event or Problem Description
Revision surgery - due to the patient's subscap failing and requiring a revision to a reverse to stabilize and regain normal function.
Additional Manufacturer Narrative
Manufacturer narrative: the reason for this revision surgery was due to failed subscap.The previous surgery and the surgery detailed in this investigation occurred 5.1 years apart.The healthcare professional indicated there was serious risk to the patient.There was no delay in surgery and another suitable device was available for use.The revision surgery was completed as intended.This investigation is limited in scope as the item(s) associated with this investigation was not returned to djo surgical - austin for examination.A review of the implant device history records (dhr), shows that the reported component(s) used in the previous surgery, when released for use, met design and manufacturing requirements.There were no non-conforming material reports associated with the product(s) that may have contributed to the reported event.The device(s) was verified to have gone through an acceptable sterilization process and was within its expiration date at the time of use during the previous surgery.Customer complaint history of the reported device(s) showed no present trends or on-going issues that are in need of review.The root cause of this complaint was a revision surgery due to failed subscap.There were no findings during this investigation that indicate that the reported device(s) was defective.No other 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 of 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 42
• Manufacturer (Section D): ENCORE MEDICAL L.P.; 9800 metric blvd; austin TX 78758 5445
• MDR Report Key: 8162676
• Report Number: 1644408-2018-01133
• Device Sequence Number: 14172857
• Product Code: KWS
• UDI-Device Identifier: 00888912024884
• UDI-Public: (01)00888912024884
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• PMA/510(K) Number: K123982
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2013
• Device Explanted Year: 2018
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 01/25/2019

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: 05/28/2018
• Device Model Number: 520-00-000
• Device Catalogue Number: 520-01-242
• Device Lot Number: 191G1057
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 11/27/2018
• Supplement Date Received by Manufacturer: 01/22/2019
• Initial Report FDA Received Date: 12/13/2018
• Supplement Report FDA Received Date: 01/25/2019
• 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 878C1237; 520-01-012, LOT 456G1082; 520-01-012, LOT 456G1082; 520-01-242, LOT 191G1057; 520-42-116, LOT 913C1032; 520-42-116, LOT 913C1032
• Outcome Attributed to Adverse Event: Other; Required Intervention
• Patient Age: 79 YR
• Patient Weight: 75