MAUDE Adverse Event Report: TORNIER INC TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX26MM STERILE; shoulder prosthesis, reverse configuration

Catalog Number	DWJ726
Medical Device Problem Codes	Loss of Osseointegration (2408); Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Pain (1994); Loss of Range of Motion (2032)
Date of Event	05/06/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Upon completion of the investigation, additional information will be provided in a supplemental report.
Event or Problem Description
It was reported that the patient underwent a right primary reverse shoulder arthroplasty.At approximately two-year follow-up, the patient presented with shoulder pain and reduced range of motion.The surgeon noted reported non-compliance with postoperative rehabilitation and a history of potential trauma while climbing in and out of a truck.During revision surgery, the glenoid component was found to be loose and dissociated from the glenoid bone and was easily removed.The humeral component remained well fixed and was retained.The polyethylene insert exhibited eccentric wear, and grey synovial tissue was observed and excised.Copious lavage was performed.New glenoid components were implanted with the addition of synthetic bone graft.A new humeral polyethylene insert was placed.The shoulder was reduced and found to be stable through range of motion.
Event or Problem Description
It was reported that the patient underwent a right primary reverse shoulder arthroplasty.At approximately two-year follow-up, the patient presented with shoulder pain and reduced range of motion.The surgeon noted reported non-compliance with postoperative rehabilitation and a history of potential trauma while climbing in and out of a truck.During revision surgery, the glenoid component was found to be loose and dissociated from the glenoid bone and was easily removed.The humeral component remained well fixed and was retained.The polyethylene insert exhibited eccentric wear, and grey synovial tissue was observed and excised.Copious lavage was performed.New glenoid components were implanted with the addition of synthetic bone graft.A new humeral polyethylene insert was placed.The shoulder was reduced and found to be stable through range of motion.
Additional Manufacturer Narrative
Correction: h6 device code, d4 lot# and h6 component code.The reported event was confirmed since images were provided and assessed by the stryker hcp.A device inspection was not possible since the affected device was not returned.Visual examination of provided pictures revealed that the peripheral screws are contained between the baseplate and glenosphere with significant bioburden covering the devices.Device identification could not be confirmed.The condition of the devices, other than the breakage of one of the peripheral screws, could also not be confirmed.Per hcp assessment of the case, the event of loosening and migration can be confirmed based on review of the provided ct images.Evidence of bone apposition suggests the implant had osseointegrated, however the purchase in the bone during implantation for the peripheral screws cannot be assessed due to the limited amount of information available.Granulomatous tissue was observed, likely related to wear particles from the polyethylene liner.The polyethylene wear and deformation are considered most likely due to loss of implant fixation rather than primary implant malalignment.Patient non-compliance may also have contributed to the event as it was noted that the patient was not following post-op physiotherapy and was removing the arm sling too early.A review of the device history for the reported lot did not indicate any abnormalities.No corrective actions are required at this time.A review of the labeling did not indicate any abnormalities.No indications of material, manufacturing or design related problems were found during the investigation.More detailed information such as clinical notes and x-rays from the initial implantation, must be available in order to determine the root cause of the complaint event.If the device is returned or if any additional information is provided, the investigation will be reassessed.

• Brand Name: TORNIER PERFORM REVERSED PERIP SCREW 5.0MMX26MM STERILE
• Common Device Name: shoulder prosthesis, reverse configuration
• Manufacturer (Section D): TORNIER INC; 10801 nesbitt avenue s; bloomington MN 55437
• Manufacturer (Section G): Tornier Inc; 10801 nesbitt avenue s; bloomington MN 55437
• Manufacturer Contact: dannielle stap ; 325 corporate drive; mahwah, NJ 07430 ; +1(201)831-5000
• MDR Report Key: 25734865
• Report Number: 0001649390-2026-00695
• Device Sequence Number: 10459769
• Product Code: PHX
• UDI-Device Identifier: 00846832091249
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K161742
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial,Followup
• Report Date (Section B): 09/16/2026

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: Lay User/Patient
• Device Catalogue Number: DWJ726
• Device Lot Number: AG3510
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 05/06/2026
• Supplement Date Received by Manufacturer: 08/19/2026
• Initial Report FDA Received Date: 07/07/2026
• Supplement Report FDA Received Date: 09/16/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 12/14/2023
• 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
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 76 YR
• Patient Sex: Male