MAUDE Adverse Event Report: ENCORE MEDICAL, L.P. TURON SHOULDER; TURON PRIMARY HUMERAL STEM, SZ 10

Model Number	520-01-010
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	04/17/2017
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The reason for this revision surgery was due to rotator cuff failure.The previous surgery and the revision detailed in this investigation occurred over 10 months 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 the hospital and not made available to djo surgical for examination.A review of the implant device history records (dhr) shows that the reported component used in the previous surgery met design and manufacturing requirements.There were no non-conforming material reports (ncmrs) associated with the product that may have contributed to the event.The device was within its expiration date at the time of use during the previous surgery.Customer complaint history of the reported device showed no present trends or on-going issues that are in need of review.There were no findings during this investigation that indicate that the reported device was the source or had a direct connection with the event.The root cause of this complaint was a revision surgery due to the rotator cuff failure.It was reported the rotator cuff failure was due to being worn out overtime.No additional information was submitted with the complaint regarding pre-existing conditions of the patient or any activities that may have contributed to the event and hence a definitive root cause cannot be determined.Inventory containment is not required as there are no indications of a product or process issue affecting implant safety or effectiveness.

• Brand Name: TURON SHOULDER
• Common Device Name: TURON PRIMARY HUMERAL STEM, SZ 10
• Manufacturer (Section D): ENCORE MEDICAL, L.P.; 9800 metric blvd.; austin TX 78758
• MDR Report Key: 6567673
• Report Number: 1644408-2017-00343
• Device Sequence Number: 13733896
• Product Code: KWS
• UDI-Device Identifier: 00888912024891
• UDI-Public: (01)00888912024891
• Combination Product (Y/N): N
• Initial Reporter State: UT
• Initial Reporter Country: US
• PMA/510(K) Number: K080402
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Device Explanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 07/29/2017

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: 05/27/2022
• Device Model Number: 520-01-010
• Device Catalogue Number: 520-01-010
• Device Lot Number: 455G1211
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 04/17/2017
• Supplement Date Received by Manufacturer: 06/30/2017
• Initial Report FDA Received Date: 05/15/2017
• Supplement Report FDA Received Date: 07/29/2017
• 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 878C1598; 520-01-238,LOT 190G1047; 520-42-116,LOT 913C1030
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 56 YR