MAUDE Adverse Event Report: TORNIER INC ASCEND HUMERAL STEM SIZE 1C BOM; PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, CEMENTED

Catalog Number	503301C
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Joint Laxity (4526); Joint Impingement (4834)
Date of Event	09/08/2025
Type of Reportable Event	Serious Injury
Event or Problem Description
The manufacturer received a report from the national joint registry that contains unpublished collected data on the usage and the outcomes of the shoulder joint replacement.The report details analysis provided for revision procedures performed between 2017 to 2025.During the review of the report, it was identified that on (b)(6) 2025, a patient required revision surgery due to stiffness, impingement, native glenoid surface erosion and lateral humeral wear, which was not previously reported to the manufacturer.
Additional Manufacturer Narrative
The reported event could not be confirmed, since the device was not returned for evaluation, and no other additional information was received from the national joint registry.More detailed information about the patient's medical history, the event details and the involved device(s) must be available to determine the root cause.If any additional information becomes available, the investigation will be reopened and re-evaluated accordingly.Please note, that reports received from the national joint registry are not published reports and therefore web link is not available.
Additional Manufacturer Narrative
This supplemental mdr is submitted to correct the initial report submitted on 10-dec-2025.Upon completion of the investigation, it was determined that the reported item cannot be associated with an inspyre implant.Based on these findings, the complaint has been cancelled, and mdr 0001649390-2025-00939 does not meet the criteria for reportability under 21 cfr part 803.No further medical device reporting is required for this event.
Event or Problem Description
The manufacturer received a report from the national joint registry that contains unpublished collected data on the usage and the outcomes of the shoulder joint replacement.The report details analysis provided for revision procedures performed between 2017 to 2025.During the review of the report, it was identified that on (b)(6) 2025 a patient required revision surgery due to stiffness, impingement, native glenoid surface erosion and lateral humeral wear, which was not previously reported to the manufacturer.

• Brand Name: ASCEND HUMERAL STEM SIZE 1C BOM
• Common Device Name: PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, CEMENTED
• Manufacturer (Section D): TORNIER INC; 10801 nesbitt avenue s; bloomington MN 55437
• Manufacturer (Section G): WRIGHT MEDICAL CORK (TORNIER ORTHOPEDICS IRELAND LTD); harnetts cross; macroom, co. cork MN NA ; EI NA
• Manufacturer Contact: dannielle stap ; 325 corporate drive; mahwah, NJ 07430 ; 2018315000
• MDR Report Key: 23768670
• Report Number: 0001649390-2025-00939
• Device Sequence Number: 9750541
• Product Code: KWS
• UDI-Device Identifier: 00846832004416
• UDI-Public: 00846832004416
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• PMA/510(K) Number: K150583
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Device Explanted Year: 2025
• Reporter Type: Manufacturer
• Report Source: Other
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 01/22/2026

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: 503301C
• Device Lot Number: 5850AO
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 11/17/2025
• Supplement Date Received by Manufacturer: 01/20/2026
• Initial Report FDA Received Date: 12/10/2025
• Supplement Report FDA Received Date: 01/22/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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: 63 YR
• Patient Sex: Male