MAUDE Adverse Event Report: STRYKER GMBH T2 ALPHA TIBIA - TIBIAL NAIL D10X300MM; ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

Catalog Number	23411030S
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Nonunion/Delayed-union Bone Fracture (2369)
Date of Event	08/04/2025
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Once the investigation is completed, any additional information will be reported in a supplemental report.
Event or Problem Description
As reported: "planned t2 alpha tibial nail revision for non-united fracture.Planned for synthes nail to be used for revision alongside synthes small frag plate.Stryker t2 alpha tibial 10x300mm nail currently implanted.Original surgery on (b)(6) 2025.Complication during original surgery, quad tendon split from suprapatellar approach, change to infrapatellar." update on 22/8: the revision procedure did not end up going ahead as the patient was not covered by insurance.
Additional Manufacturer Narrative
Correction: please refer to section d9 the device was not returned.The reported event could not be confirmed since the device was not returned for evaluation and no other evidences were provided.More detailed information about the complaint event as well as the affected device must be available in order to determine the root cause of the complaint event.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.If the device is returned or if any additional information is provided, the investigation will be reassessed.
Event or Problem Description
As reported: "planned t2 alpha tibial nail revision for non-united fracture.Planned for synthes nail to be used for revision alongside synthes small frag plate.Stryker t2 alpha tibial 10x300mm nail currently implanted.Original surgery on (b)(6) 2025.Complication during original surgery, quad tendon split from suprapatellar approach, change to infrapatellar." update on 22/8: the revision procedure did not end up going ahead as the patient was not covered by insurance.

• Brand Name: T2 ALPHA TIBIA - TIBIAL NAIL D10X300MM
• Common Device Name: ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
• Manufacturer (Section D): STRYKER GMBH; bohnackerweg 1; postfach; selzach 2545 ; SZ 2545
• Manufacturer (Section G): STRYKER TRAUMA KIEL; prof. kuentscher-strasse 1-5; schoenkirchen/kiel D-242 32; GM D-24232
• Manufacturer Contact: dannielle stap ; 325 corporate drive; mahwah, NJ 07430 ; 2018315000
• MDR Report Key: 22931719
• Report Number: 0008031020-2025-01437
• Device Sequence Number: 18739482
• Product Code: HSB
• UDI-Device Identifier: 07613327290967
• UDI-Public: (01)07613327290967(11)221010(17)320930(10)K0D4036
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K193308
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• Device Explanted Year: 2025
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 11/12/2025

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: 23411030S
• Device Lot Number: K0D4036
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 08/04/2025
• Supplement Date Received by Manufacturer: 10/15/2025
• Initial Report FDA Received Date: 09/02/2025
• Supplement Report FDA Received Date: 11/12/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 10/10/2022
• 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: 42 YR
• Patient Sex: Female