MAUDE Adverse Event Report: ENCORE MEDICAL L.P. TURON SHOULDER; TURON PRIMARY HUMERAL STEM, SZ 12

Model Number	520-01-012
Health Effect - Clinical Codes	Bone Fracture(s) (1870); Seizures (2063)
Date of Event	05/03/2017
Type of Reportable Event	Serious Injury
Event or Problem Description
Revision surgery - after the initial surgery the patient had a seizure and fractured the stem.The stem needed to be replaced due to the fall.
Additional Manufacturer Narrative
Manufacturer narrative: the reason for this revision surgery was the stem fractured.The in-vivo length of patient service for the implant was 7 days.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 device history records (dhrs) revealed no discrepancies or issues with the manufacturing of this part.All critical dimensions, design criteria and specifications in effect at the time the part was manufactured were met.The product complaint report history was reviewed and no trends or on-going issues were deemed as present or in need of review.This event is deemed as non-product related.The root cause for the fractured stem was the patient had a seizure and fell.It was reported the stem need to replaced due to the fall.Inventory containment is not required since 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 12
• Manufacturer (Section D): ENCORE MEDICAL L.P.; 9800 metric blvd.; austin TX 78758 5445
• MDR Report Key: 6606069
• Report Number: 1644408-2017-00410
• Device Sequence Number: 533495
• Product Code: KWS
• UDI-Device Identifier: 00888912024907
• UDI-Public: (01)00888912024907
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: K080402
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 07/18/2017

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: 11/18/2022
• Device Model Number: 520-01-012
• Device Catalogue Number: 520-01-012
• Device Lot Number: 456G1232
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 05/03/2017
• Supplement Date Received by Manufacturer: 06/19/2017
• Initial Report FDA Received Date: 06/01/2017
• Supplement Report FDA Received Date: 07/18/2017
• 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 878C1657; 520-46-020,LOT 919C1068
• Outcome Attributed to Adverse Event: Required Intervention