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

Model Number 520-01-242

Device Problems Device Operates Differently Than Expected (2913); Torn Material (3024)

Patient Problem No Code Available (3191)

Event Date 07/10/2017

Event Type  Injury  

Event Description

Revision surgery - due to failed total shoulder with cuff tear which required a reverse to be put in.

Manufacturer Narrative

The reason for this revision surgery was a failed total shoulder with cuff tear.The in-vivo length of patient service for the implant was 5.2 years.There is no information in this complaint about any patient injuries, activities, or accidents that may have contributed to the need for this revision surgery.There are no reported pre-existing patient health conditions.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 this event was the patient had failed total shoulder with cuff tear which required a reverse shoulder system.The scope of this investigation is limited without having the explanted parts available to djo surgical for evaluation.Other conditions relating to this event could not be determined with confidence.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
• Type of Device: TURON PEGGED GLENOID IMPLANT, SIZE 42
• Manufacturer (Section D): ENCORE MEDICAL L.P.; 9800 metric blvd.; austin TX 78758 5445
• Manufacturer (Section G): ENCORE MEDICAL L.P.; 9800 metric blvd.; austin TX 78758 5445
• Manufacturer Contact: teffany hutto ; 9800 metric blvd.; austin, TX 78758-5445
• MDR Report Key: 6774626
• MDR Text Key: 82070403
• Report Number: 1644408-2017-00652
• Device Sequence Number: 1
• Product Code: KWS
• UDI-Device Identifier: 00888912024952
• UDI-Public: (01)00888912024952
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K123982
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 10/12/2017

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
• Device Operator: Health Professional
• Device Expiration Date: 08/20/2016
• Device Model Number: 520-01-242
• Device Catalogue Number: 520-01-242
• Device Lot Number: 191G1024
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Initial Date Manufacturer Received: 07/10/2017
• Initial Date FDA Received: 08/08/2017
• Supplement Dates Manufacturer Received: 09/20/2017
• Supplement Dates FDA Received: 10/18/2017
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 08/24/2011
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: 520-00-000,LOT 878C1095; 520-01-010,LOT 455G1024; 520-42-016,LOT 909C1003
• Patient Outcome(s): Hospitalization; Required Intervention
• Patient Age: 86 YR