MAUDE Adverse Event Report: ENCORE MEDICAL L.P. METAL/METAL HIP SYSTEM; LINER, METAL-METAL 34MM NEUTRAL MP7

Model Number	497-34-000
Health Effect - Clinical Codes	Pain (1994); Toxicity (2333)
Date of Event	07/06/2014
Type of Reportable Event	Serious Injury
Event or Problem Description
Revision surgery - due to left groin pain and elevated metal levels.
Additional Manufacturer Narrative
Product complaints that were identified during litigation were previously sent to an employee that is no longer with the company.This information was not transferred over.Once this complaint was identified, it was immediately processed.
Additional Manufacturer Narrative
Manufacturer narrative: the reason for this revision surgery was due to left groin pain and elevated metal levels.The previous surgery and the revision detailed in this investigation occurred 3.6 years apart.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 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 reported event.The device 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 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 left groin pain and elevated metal levels.There were no findings during this investigation that indicate that the reported device was defective.There are multiple factors that may contribute to an event that are outside of the control of djo surgical.Inventory containment is not required as there are no indications of a product or process issue affecting implant safety or effectiveness.
Additional Manufacturer Narrative
Corrected data: initially reported 5-jun-2017 as the awareness date, this follow-up is correcting that date.The correct awareness date should be 2-nov-2016.

• Brand Name: METAL/METAL HIP SYSTEM
• Common Device Name: LINER, METAL-METAL 34MM NEUTRAL MP7
• Manufacturer (Section D): ENCORE MEDICAL L.P.; 9800 metric blvd; austin TX 78758 5445
• MDR Report Key: 7437126
• Report Number: 1644408-2018-00354
• Device Sequence Number: 19147835
• Product Code: KWA
• UDI-Device Identifier: 00888912087308
• UDI-Public: (01)00888912087308
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• PMA/510(K) Number: K040354
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2010
• Device Explanted Year: 2014
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup,Followup
• Report Date (Section B): 06/05/2018

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: 03/28/2015
• Device Model Number: 497-34-000
• Device Catalogue Number: 499-34-007
• Device Lot Number: A1000002
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Initial Date Received by Manufacturer: 06/05/2017
• Supplement Date Received by Manufacturer: 06/05/2017; 05/24/2018; 06/05/2018
• Initial Report FDA Received Date: 04/17/2018
• Supplement Report FDA Received Date: 04/17/2018; 05/25/2018; 06/05/2018
• 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: 411-00-035, LOT 903B1013; 411-00-035, LOT 903B1013; 427-01-120, LOT A1000000; 427-01-120, LOT A1000000; 430-01-052, LOT 284C1011; 430-01-052, LOT 284C1011; 497-34-000, LOT 636C1003; 499-34-007, LOT A1000002; 411-00-035, LOT 903B1013; 427-01-120, LOT A1000000; 430-01-052, LOT 284C1011; 499-34-007, LOT A1000002
• Outcome Attributed to Adverse Event: Required Intervention