MAUDE Adverse Event Report: ENCORE MEDICAL L.P. BIOLOX DELTA HIP; HEAD, FEMORAL, CERAMIC, BILOX DELTA, 36MM NEUTRAL

Model Number	931-36-252
Health Effect - Clinical Code	Joint Dislocation (2374)
Date of Event	08/10/2019
Type of Reportable Event	Serious Injury
Event or Problem Description
Revision surgery - due to dislocation.
Additional Manufacturer Narrative
Manufacturer narrative: the reason for this revision surgery was reported as dislocation.The previous surgery and the surgery detailed in this event occurred 6 years and 4 months apart.The healthcare professional indicated there was a significant adverse event.There was no delay in surgery and another suitable device was available for use.The revision surgery was completed as intended.The device was not returned and not made available to djo surgical for examination.A review of the device history record show that the reported component used in the previous surgery, when released for use, met design and manufacturing requirements.There were no nonconforming material reports 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 the previous surgery.Customer complaint history of the reported device showed no present trends or on-going issues that are needing a review.The root cause of this complaint was a revision surgery due to dislocation.There were no findings during this evaluation that indicate the reported devices were defective.No 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 the control of djo surgical such as poor bone density, patient bone deterioration, inadequate soft tissue support, patient non-compliance with medical instructions, excessive range of motion, patient activities or trauma.There are no indications of a product or process issue affecting implant safety or effectiveness.

• Brand Name: BIOLOX DELTA HIP
• Common Device Name: HEAD, FEMORAL, CERAMIC, BILOX DELTA, 36MM NEUTRAL
• Manufacturer (Section D): ENCORE MEDICAL L.P.; 9800 metric blvd; austin TX 78758 5445
• MDR Report Key: 8971416
• Report Number: 1644408-2019-00914
• Device Sequence Number: 2950809
• Product Code: LZO
• UDI-Device Identifier: 00888912099509
• UDI-Public: (01)00888912099509
• Combination Product (Y/N): N
• Initial Reporter State: NV
• Initial Reporter Country: US
• PMA/510(K) Number: K082844
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2013
• Device Explanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 10/15/2019

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: 03/31/2018
• Device Model Number: 931-36-252
• Device Catalogue Number: 400-03-362
• Device Lot Number: 866B1052
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 08/10/2019
• Supplement Date Received by Manufacturer: 09/16/2019
• Initial Report FDA Received Date: 09/06/2019
• Supplement Report FDA Received Date: 10/16/2019
• 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: (B)(4), LOT 690F1062; (B)(4), LOT 866B1052; 400-03-362, LOT 866B1052
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 74 YR