MAUDE Adverse Event Report: TREACE MEDICAL CONCEPTS, INC. 2MM X 40MM OLIVE WIRE WITH THREADED TIP

Model Number	1405-2015
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	Foreign Body In Patient (2687)
Date of Event	11/02/2022
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
It was reported that the tip of an olive wire broke off and was retained in the patient's bone during a bunion procedure on (b)(6) 2022.The olive wire is provided to customers within a sterile kit (sk34) and marked single use.The udi referenced is for the sterile kit, sk34, that the product is distributed within.The device was not returned for evaluation.The device history records for all possible parts and lots were reviewed, and no issues were identified during the manufacture and release of the device that could have contributed to what was reported.Additional information indicates that while drilling, the surgeon believes he hit the compression (olive) wire.The case was successfully completed with no additional patient outcomes.Based on the available information, the most likely cause of what was reported is that the olive wire broke due to impact with another device.The product is manufactured with implant grade material and no report of impact/injury or case delay, nor have any adverse events previously been reported as a result of this failure to date.Although the company has determined that the subject event in this mdr is unlikely to result in a serious injury if it recurred, the company has decided to file this mdr in an abundance of caution and to ensure full compliance with 21 cfr part 803.The company will supplement this mdr as necessary and appropriate.
Event or Problem Description
It was reported that the tip of an olive wire broke off and was retained in the patient's bone during a bunion procedure on (b)(6) 2022.The case was successfully completed with no additional patient outcomes.

• Brand Name: 2MM X 40MM OLIVE WIRE WITH THREADED TIP
• Common Device Name: OLIVE WIRE
• Manufacturer (Section D): TREACE MEDICAL CONCEPTS, INC.; 100 palmetto park place; ponte vedra FL 32081
• Manufacturer (Section G): TREACE MEDICAL CONCEPTS, INC.; 100 palmetto park place; ponte vedra FL 32081
• Manufacturer Contact: uriza shums ; 100 palmetto park place; ponte vedra, FL 32081 ; 9043735940
• MDR Report Key: 15911962
• Report Number: 3011623994-2022-00118
• Device Sequence Number: 5486846
• Product Code: HWE
• UDI-Device Identifier: 00853114006273
• UDI-Public: 00853114006273
• Combination Product (Y/N): N
• Initial Reporter State: KS
• Initial Reporter Country: US
• PMA/510(K) Number: N/A-CLASS I
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2022
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Distributor
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 12/02/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 10/14/2024
• Device Model Number: 1405-2015
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 11/02/2022
• Initial Report FDA Received Date: 12/03/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 10/14/2021
• 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
• Patient Age: 32 YR
• Patient Sex: Female