MAUDE Adverse Event Report: ENCORE MEDICAL L. P. TAPERFILL FEMORAL HIP STEM; TAPERFILL HIP STEM, LATERAL OFFSET, SIZE 19

Model Number	425-97-019
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	04/09/2021
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Manufacturer narrative: additional reporting on this event will be provided as a supplemental report to this document as soon as it becomes available.
Event or Problem Description
Revision surgery - due to patient had a femur fracture after a total hip done a year before with a djo hip.Taperfill stem size 19 was removed and an exprt stem was used to replace.Per surgeon, taperfill stem was not reason for the revision.
Additional Manufacturer Narrative
The reason for this revision surgery was reported as femur fracture.The previous surgery and the surgery detailed in this event occurred 8 months and 3 weeks apart.The healthcare professional indicated there was a life-threatening to the patient.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.There was a nonconformance associated with the main part #425-97-019 taperfill hip stem, lateral offset, size 19 which documents that out of 25 parts lot, 3 parts were rejected, out of which 2 parts were rejected due to rework in porous coating and 1 part was rejected and scrapped due to inconsistent surface finish.All other items in the lot were met with fit, form 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 femur fracture.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, patient bone deterioration, 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
See b2: life-threatening event was checked of in error on follow-up #: 1.Confirmed with represesentative this was not a life-threatening event.Additional reporting on this event will be provided as a supplemental report to this document if it becomes available.

• Brand Name: TAPERFILL FEMORAL HIP STEM
• Common Device Name: TAPERFILL HIP STEM, LATERAL OFFSET, SIZE 19
• Manufacturer (Section D): ENCORE MEDICAL L. P.; 9800 metric blvd.; austin TX 78758 5445
• MDR Report Key: 11758780
• Report Number: 1644408-2021-00398
• Device Sequence Number: 17266196
• Product Code: LPH
• UDI-Device Identifier: 00888912078764
• UDI-Public: (01)00888912078764
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K130099
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2020
• Device Explanted Year: 2021
• 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): 06/07/2021

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: 08/31/2020
• Device Model Number: 425-97-019
• Device Catalogue Number: 425-97-019
• Device Lot Number: 183R1004
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 04/09/2021
• Supplement Date Received by Manufacturer: 05/14/2021; 06/07/2021
• Initial Report FDA Received Date: 05/02/2021
• Supplement Report FDA Received Date: 06/03/2021; 06/07/2021
• 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: 400-03-362, LOT 866B1610
• Outcome Attributed to Adverse Event: Life Threatening; Required Intervention
• Patient Age: 34 YR