MAUDE Adverse Event Report: ENCORE MEDICAL L.P LINEAR HIP; LINEAR, LATERAL, REDUCED NECK, SZ 13, W/P2 COATING

Model Number	425-99-013
Health Effect - Clinical Code	Bone Fracture(s) (1870)
Date of Event	10/08/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Additional reporting on this event will be provided as a supplemental report to this document if it becomes available.
Event or Problem Description
Revision surgery - patient had a proximal femur fracture.Removed stem and put in exprt hip with cables.
Additional Manufacturer Narrative
Manufacturer narrative: the reason for this revision surgery was reported as proximal femur fracture.The previous surgery and the surgery detailed in this event occurred 3 years and 6 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 record (dhr) shows that the reported component used in the previous surgery, when released for use, met design and manufacturing requirements.There was an ncmr#25109 associated with the main part #425-99-013, linear, lateral, reduced neck, sz 13, w/p2 coating, which documents that out of 10 parts lot, 4 parts were rejected due to undersized slot and ding/belt marks on neck.Later the rejected parts were reworked and accepted after proper justification.All other items in the lot were met with the design, fit and function requirements.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 proximal femur fracture.There were no findings during this evaluation that indicate the reported devices were defective.No other 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 the event that are outside the control of djo surgical such as poor bone density, inadequate soft tissue support, prolonged overhead activities, patient activities or trauma.There are no indications of a product or process issue affecting implant safety or effectiveness.Additional reporting on this event will be provided as a supplemental report to this document if it becomes available.
Additional Manufacturer Narrative
Corrected data: see g1 - new conact for encore medical l.P.Additional reporting on this event will be provided as a supplemental report to this document if it becomes available.

• Brand Name: LINEAR HIP
• Common Device Name: LINEAR, LATERAL, REDUCED NECK, SZ 13, W/P2 COATING
• Manufacturer (Section D): ENCORE MEDICAL L.P; 9800 metric blvd; austin,tx 78758-5445
• MDR Report Key: 10792950
• Report Number: 1644408-2020-01004
• Device Sequence Number: 2954365
• Product Code: LPH
• UDI-Device Identifier: 00888912078993
• UDI-Public: (01)00888912078993
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K120241
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2020
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 03/21/2021

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: 01/31/2021
• Device Model Number: 425-99-013
• Device Catalogue Number: 425-99-013
• Device Lot Number: 578G1016
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 10/08/2020
• Supplement Date Received by Manufacturer: 11/16/2020; 11/16/2020
• Initial Report FDA Received Date: 11/05/2020
• Supplement Report FDA Received Date: 12/15/2020; 03/21/2021
• 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 903B1791; 411-00-035 LOT 903B1971; 497-40-000 LOT 641C1083; 411-00-035 LOT 903B1791; 497-40-000 LOT 641C1083
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 77 YR