MAUDE Adverse Event Report: ENCORE MEDICAL L.P. EPIK UNI KNEE; FEMUR, EPIK, SIZE8 LM/RL

Model Number 200-01-108

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problems Pain (1994); Joint Laxity (4526)

Event Date 11/16/2022

Event Type  Injury  

Event Description

Revision surgery, unaware of symptoms, could of been instability or pain possibly.Upon removal the femoral component appeared to be loose.

Manufacturer Narrative

The reason for this revision surgery was reported as instability, pain and loosening.The previous surgery and the surgery detailed in this event occurred 7 years and 9 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 devices were disposed of at hospital and not made available to djo surgical for examination.A review of the device history records (dhr) show that the reported components used in the previous surgery, when released for use, met design and manufacturing requirements and showed no non-conforming material reports (ncmr) associated with the main contributor component listed in the complaint.The devices were verified to have gone through an acceptable sterilization process and were within its expiration date at the time of the previous surgery.Customer complaint history of the reported devices 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 instability, pain and loosening.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 also contribute to an event that are outside the control of djo surgical such as poor bone density, inadequate soft tissue support, patient activities.There are no indications of a product or process issue affecting implant safety or effectiveness.

• Brand Name: EPIK UNI KNEE
• Type of Device: FEMUR, EPIK, SIZE8 LM/RL
• 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: james mcmahon ; 9800 metric blvd; austin, tx 78758-5445
• MDR Report Key: 15908927
• MDR Text Key: 304774768
• Report Number: 1644408-2022-01610
• Device Sequence Number: 1
• Product Code: HRY
• UDI-Device Identifier: 00888912108928
• UDI-Public: (01)00888912108928
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K020741
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Company Representative
• Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date: 12/02/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/02/2022
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Health Professional
• Device Expiration Date: 08/31/2015
• Device Model Number: 200-01-108
• Device Catalogue Number: 200-01-108
• Device Lot Number: 54015563
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 11/16/2022
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 09/02/2009
• 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: 300-01-040 LOT 068B1004; 340-40-009 LOT 59600620
• Patient Outcome(s): Required Intervention
• Patient Age: 65 YR
• Patient Sex: Male