MAUDE Adverse Event Report: Encore Medical L.P DJO SURGICAL; AltiVate Anatomic, All-Poly Pegged Glenoid, Size 42, E-Plus

Catalog Number	521-07-242
Medical Device Problem Code	No Apparent Adverse Event (3189)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	07/20/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The agent reported, "failure to thrive.Age 72 gender female." the previous surgery and the surgery detailed in this event occurred 1 year, 1 month, 11 days apart.Item number: 521-07-242, item description: altivate anatomic, all-poly pegged glenoid, size 42, e-plus, lot#: 891u1377, part revision: b, product type: shoulder, manufacture date: 10-jan-2025, expiration date: 07-jan-2030.This evaluation is limited in scope as the item(s) associated with this investigation was not returned to djo surgical - austin for examination.The surgery was completed as intended.If additional information regarding the reported event is submitted at a future date, this investigation will be re-evaluated.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 were no findings during this evaluation that indicate that the reported device(s) was defective.The surgeon performed this procedure to remedy the patient's condition.No further action is deemed necessary.Root cause: the root cause of this complaint was a revision surgery due to failure to thrive.There are multiple factors that may contribute to this event that are outside of the control of enovis surgical.Containment: inventory containment is not required as there are no indications of a product or process issue affecting implant safety or effectiveness.The revision surgery was completed successfully.Device history records review: a review of the device history records (dhr) shows that the reported components used in the previous surgery, when released for use, met design and manufacturing requirements.There was an ncmr-74499 associated with the concomitant part 520-14-000, altivate anatomic, short humeral stem, 14mm, which documented that out of (b)(4) parts in the lot, 32 parts were identified for rework due to an internal process issue.The material was assessed as low risk and determined to be reworkable with no new unacceptable risk to performance or safety.The rejected parts were subsequently reworked and accepted after proper justification.All other items in the lot met fit, form, and function requirements.The devices were verified to have gone through an acceptable sterilization process and were within their expiration date at the time of the previous surgery.Complaint history: customer complaint history of the reported device(s) showed no present trends or ongoing issues that need review.
Event or Problem Description
Revision surgery - due to unknown revision reason.

• Brand Name: DJO SURGICAL
• Common Device Name: AltiVate Anatomic, All-Poly Pegged Glenoid, Size 42, E-Plus
• Manufacturer (Section D): Encore Medical L.P; 9800 metric blvd.; austin TX 78758
• Manufacturer (Section G): Encore Medical L.P; 9800 metric blvd.; austin TX 78758
• Manufacturer Contact: stacey bonnell ; 9800 metric blvd.; austin, TX 78758
• MDR Report Key: 50168676
• Report Number: 1644408-2026-01495
• Device Sequence Number: 12075795
• Product Code: PAO
• UDI-Device Identifier: 00190446178361
• UDI-Public: 00190446178361
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• PMA/510(K) Number: K162024
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• Device Explanted Year: 2026
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 08/06/2026

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 Catalogue Number: 521-07-242
• Device Lot Number: 891U1377
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/20/2026
• Initial Report FDA Received Date: 08/07/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 01/10/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 520-07-000 Lot. 888U1845A.; 520-14-000 Lot. 853U1373.; 520-46-318 Lot. 878U1065.
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 72 YR
• Patient Sex: Female