MAUDE Adverse Event Report: Stryker Orthopaedics-Mahwah TRIDENT 0 DEG X3 INSERT 32D; Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

Catalog Number	723-00-32D
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	04/23/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
The following information was provided: it was reported that: aseptic loosening, infection of hip joint post-operatively.
Additional Manufacturer Narrative
The following devices were also listed in this report: tridentii tritanium cluster50d; cat # 702-04-50d; lot # 19605251a; delta v-40 ceramic head 32/0; cat # 6570-0-132; lot # 22035152; md universal cement restrictor; cat # b000-0240; lot # 6m10574; 6.5 mm low profile hex screw 30 mm; cat # 7030-6530; lot # hfgh; 6.5 mm low profile hex screw 25 mm; cat # 7030-6525; lot # hpze; exeter v40 stem 37.5 mm no1l125; cat # 0580-3-371; lot # g8598880.It cannot be determined which, if any of these devices may have caused or contributed to the patient's experience.Review of the device history records indicate that devices were manufactured and accepted into final stock with no reported discrepancies.There has been similar event(s) for the lot referenced.If additional information is received, it will be provided in a supplemental report upon completion of the investigation.

• Brand Name: TRIDENT 0 DEG X3 INSERT 32D
• Common Device Name: Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
• Manufacturer (Section D): Stryker Orthopaedics-Mahwah; 325 corporate drive; mahwah NJ 07430
• Manufacturer (Section G): Stryker Orthopaedics-Mahwah; 325 corporate drive; mahwah NJ 07430
• Manufacturer Contact: anna ryan ; raheen business park; limerick, NJ NA ; EI NA ; +353()61498200
• MDR Report Key: 25240256
• Report Number: 0002249697-2026-00431
• Device Sequence Number: 16077405
• Product Code: JDI
• UDI-Device Identifier: 07613327342710
• UDI-Public: 07613327342710
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K250989
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2024
• Device Explanted Year: 2026
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 09/21/2026

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: 723-00-32D
• Device Lot Number: YR534W
• 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: 04/23/2026
• Supplement Date Received by Manufacturer: 09/10/2026
• Initial Report FDA Received Date: 05/21/2026
• Supplement Report FDA Received Date: 09/21/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 01/24/2024
• 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; Hospitalization
• Patient Age: 23 YR
• Patient Sex: Unknown