MAUDE Adverse Event Report: ENCORE MEDICAL L.P. FMP HIP; LINER, LOCKING RING, CONSTRAINED

Model Number	436-28-000
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	08/13/2019
Type of Reportable Event	Serious Injury
Event or Problem Description
Revision surgery - locking ring broke.Patient had to have a revision.The surgeon called biomet for the revision so we were not notified about the case.
Additional Manufacturer Narrative
The reason for this revision surgery was reported as locking ring broke.The previous surgery and the surgery detailed in this event occurred 1.8 years 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 device was disposed of at the hospital and not made available to djo surgical for examination.The surgeon performed this procedure to remedy the patient's condition.No further action is deemed necessary.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 broken locking ring.There were no findings during this evaluation 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.There was no information submitted with this complaint about any patient activities, accidents, or medical contraindications that may have contributed to the reported event.There was no information submitted with this complaint about any patient activities, accidents, or medical contraindications that may have contributed to the reported event.

• Brand Name: FMP HIP
• Common Device Name: LINER, LOCKING RING, CONSTRAINED
• Manufacturer (Section D): ENCORE MEDICAL L.P.; 9800 metric blvd; austin, tx 78758-5445
• MDR Report Key: 9150839
• Report Number: 1644408-2019-00951
• Device Sequence Number: 16837816
• Product Code: KWZ
• UDI-Device Identifier: 00888912085663
• UDI-Public: (01)00888912085663
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K023794
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• 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): 11/06/2019

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: 07/31/2020
• Device Model Number: 436-28-000
• Device Catalogue Number: 436-28-000
• Device Lot Number: 496C1050
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 09/05/2019
• Supplement Date Received by Manufacturer: 09/05/2019
• Initial Report FDA Received Date: 10/03/2019
• Supplement Report FDA Received Date: 11/06/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 61 YR