MAUDE Adverse Event Report: SMITH & NEPHEW, INC. INTERTAN SUBTROC LAG 11 X 90; NAIL, FIXATION, BONE

Catalog Number	71678090
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	Injury (2348)
Date of Event	01/22/2019
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that revision surgery was performed due to broken intertan and the non-union subtrochanteric fracture of the left hip, femoral neck shortening, mal reduction.
Additional Manufacturer Narrative
The associated trigen screw, intertan nail and subtroch lag screw were returned and evaluated.A lab analysis conducted during this investigation indicated that the nail showed burnishing, damage to distal slot and polished fracture surface on distal and proximal nail fragments.The trigen screw showed the tip is missing.Microscopic examination of the devices showed beach marks on the surface of the screw.Fatigue striations are observed on the fractured surface of the nail and the screw indicating a fatigue fracture.The nail and screw fractured by the initiation and subsequent propagation of fatigue cracking.For the nail, the fracture likely initiated on the lateral side of the part through the lag screw hole.The fatigue cracking eventually propagated to an extent that the remaining cross-sectional area of the nail could not bear the imposed patient loading, which led to an overload fracture of the nail.Fatigue cracking is caused by the nail bearing cyclic (i.E.Repeated) stresses in excess of the material endurance limit for an extended period of time.These excessive cyclic stresses may be caused by any number of conditions, including but not limited to excessive patient activity levels prior to full bone union, applications of loads in excess of the material¿s strength, and/or poor bone quality.No deviation was found during a review of the manufacturing records for the listed batches.A review of the complaint history for the listed parts revealed no prior complaints for the listed failure mode with the same batch number.Our clinical evaluation noted that the x-rays provided confirm the non-union of the previous femoral fracture.The future impact to the patient beyond the revision cannot be determined.No further investigation warranted for this complaint; however we will continue to monitor for future complaints and investigate as necessary.Should additional information be received, the complaint will be reopened.

• Brand Name: INTERTAN SUBTROC LAG 11 X 90
• Common Device Name: NAIL, FIXATION, BONE
• Manufacturer (Section D): SMITH & NEPHEW, INC.; 1450 brooks road; memphis TN 38116
• MDR Report Key: 8329932
• Report Number: 1020279-2019-00536
• Device Sequence Number: 2284796
• Product Code: JDS
• UDI-Device Identifier: 03596010565297
• UDI-Public: 03596010565297
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K040212
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2015
• Device Explanted Year: 2019
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 05/20/2019

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 Expiration Date: 01/20/2024
• Device Catalogue Number: 71678090
• Device Lot Number: 13MT37468
• Initial Date Received by Manufacturer: 01/22/2019
• Supplement Date Received by Manufacturer: 01/22/2019
• Initial Report FDA Received Date: 02/11/2019
• Supplement Report FDA Received Date: 05/20/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Hospitalization; Required Intervention