MAUDE Adverse Event Report: ENCORE MEDICAL L.P. ALTIVATE ANATOMIC SHOULDER; ALTIVATE ANATOMIC, NEUTRAL HUMERAL HEAD, 42X16

Model Number	520-42-216
Health Effect - Clinical Code	Loss of Range of Motion (2032)
Date of Event	08/07/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The reason for this revision surgery was reported as limiting range of motion.The previous surgery and the surgery detailed in this event occurred 1.5 years apart.The healthcare professional indicated there was a significant adverse event 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 were no non-conforming material reports (ncmr) associated with the products that may have contributed to the reported event.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 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 becoming still, limiting range of motion.There were no findings during this evaluation that indicate the reported devices was 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.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.
Event or Problem Description
Revision surgery - patient was stiff minimal range of motion, went back in with smaller head and glenoid.
Additional Manufacturer Narrative
Corrected data: the root cause of this complaint was a revision surgery due to becoming stiff, limiting range of motion.There were no findings during this evaluation that indicate the reported devices was defective.No information submitted with this complaint regarding pre-existing conditions of the patient or any activities that 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 of the control of djo surgical.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.

• Brand Name: ALTIVATE ANATOMIC SHOULDER
• Common Device Name: ALTIVATE ANATOMIC, NEUTRAL HUMERAL HEAD, 42X16
• Manufacturer (Section D): ENCORE MEDICAL L.P.; 9800 metric blvd.; austin, tx 78758-5445,
• MDR Report Key: 10498122
• Report Number: 1644408-2020-00721
• Device Sequence Number: 3203639
• Product Code: KWS
• UDI-Device Identifier: 00190446176091
• UDI-Public: (01)00190446176091
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K162024
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2019
• Device Explanted Year: 2020
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 10/06/2020

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: 08/24/2023
• Device Model Number: 520-42-216
• Device Catalogue Number: 520-42-216
• Device Lot Number: 947U1016
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 08/07/2020
• Supplement Date Received by Manufacturer: 08/07/2020
• Initial Report FDA Received Date: 09/05/2020
• Supplement Report FDA Received Date: 10/06/2020
• 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: 520-07-000 LOT 888U1248
• Outcome Attributed to Adverse Event: Other; Required Intervention
• Patient Age: 47 YR