MAUDE Adverse Event Report: SMITH & NEPHEW, INC. META-NAIL TIBIAL 10MM X 34CM; NAIL, FIXATION, BONE

Catalog Number	71655134
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Implant Pain (4561)
Date of Event	02/15/2017
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Internal complaint reference: e1, g2 (report source): data collection activity was conducted retrospectively & the data has been intentionally anonymized by the third party vendor.As a result, the healthcare facility involved with this incident is unknown.Consequently, the information provided may be limited in details and lack the ability for additional due diligence.H3, h6: this complaint was opened by smith+nephew to document a patient complication identified through the review of clinical evidence from post market clinical data collection activities that includes reference to the use of a smith+nephew product.The reported issue(s) relate to known inherent procedural risks that are appropriately documented in our risk files.Smith+nephew will continue to monitor trends in accordance with our post-market surveillance process and take necessary action as required if anticipated severity and/or occurrence rates are exceeded.Smith+nephew has no reason to suspect that the product failed to meet any specifications at the time of manufacture.Based on our review of all currently available information, we are unable to confirm a relationship between the reported event and the device or identify a definitive root cause.However, as the use of our product cannot be excluded as a potential cause or contributory factor to the reported issue, we are conservatively submitting this report in accordance with applicable regulations.If additional information becomes available that alters the conclusions of this report, a follow-up report will be submitted as required.
Event or Problem Description
It was reported that, following a right imn fixation surgery performed on (b)(6) 2016 due to a displaced comminuted fracture of shaft of the tibia, the patient required the remove of a distal interlocking screw as well as one of the proximal locking screw due to symptomatic hardware.The surgeon didn't remove all the hardware as there was not complete consolidation of the right tibial shaft.This information was collected retrospectively as part of a post-market clinical follow up (pmcf) activity and is provided in an anonymized format; therefore, no further information available.
Additional Manufacturer Narrative
H11.Corrected catalog number of the device in d4.

• Brand Name: META-NAIL TIBIAL 10MM X 34CM
• Common Device Name: NAIL, FIXATION, BONE
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 1450 brooks rd.; memphis TN 38116
• Manufacturer (Section G): SMITH & NEPHEW, INC.; 1450 brooks rd.; memphis TN 38116
• Manufacturer Contact: holly topping ; 7000 west william cannon drive; austin, TX 78735 ; 5123913905
• MDR Report Key: 20924490
• Report Number: 1020279-2024-02663
• Device Sequence Number: 5055835
• Product Code: JDS
• UDI-Device Identifier: 03596010585561
• UDI-Public: 3596010585561
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K061019
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Other,Study,Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 01/14/2025

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: 71655134
• Device Lot Number: UNKNOWN
• 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: 11/26/2024
• Supplement Date Received by Manufacturer: 01/07/2025; Not provided
• Initial Report FDA Received Date: 12/13/2024
• Supplement Report FDA Received Date: 01/07/2025; 01/14/2025
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• 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: A
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 71645030 / LOT NUMBER: UNKNOWN; 71645037 / LOT NUMBER: UNKNOWN; 71645040 / LOT NUMBER: UNKNOWN; 71645050 / LOT NUMBER: UNKNOWN; 71655134 / LOT NUMBER: UNKNOWN
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention
• Patient Age: 23 YR
• Patient Sex: Female