MAUDE Adverse Event Report: ARTHREX, INC. RADIOPAQUE FIBERTAPE CERCLAGE W/O NEEDLE; POLYETHYLENE SYNTHETIC SUTURE

Model Number	RADIOPAQUE FIBERTAPE CERCLAGE W/O NEEDLE
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	10/27/2025
Type of Reportable Event	Malfunction
Event or Problem Description
On (b)(6) 2025, a sales representative reported via email that two ar-7268r radiopaque fibertape cerclage devices were found to be defective.The devices were used to reduce a fracture of the lesser trochanter.Upon initial tensioning with minimal force, both suture limbs broke.A second cerclage was passed, resulting in the same outcome.Then a standard ar-7268t fibertape cerclage was used without issues.The faulty cerclage was removed and there was no impact to the patient.This was discovered during a procedure on (b)(6) 2025.
Additional Manufacturer Narrative
Investigation is in process.A follow-up report will be provided upon availability of additional information.
Additional Manufacturer Narrative
Additional information: b5, g3, h3, h6 the complaint device was not received for evaluation.Based on the information provided, which may include the device (if available and returned), pictures, videos, event description, and any additional information from the field, arthrex was able to conclude the most likely cause.The most likely cause of the reported failure is user error, including incorrect surgical technique during device application.These factors may have contributed to the malfunction or compromised the integrity of the implant during the procedure.Directions for use dfu-0264-eo revision 6 fibertape® and tigertape¿ cerclage sutures and radiopaque fibertape® cerclage sutures g.Precautions 1.In handling this or any other suture material, care should be taken to avoid damage from handling.Avoid crushing or crimping damage due to application of surgical instruments such as forceps or needle holders.4.Avoid wrapping the suture over sharp metal or bone graft surfaces the complaint allegation could not be confirmed, as the device was not received for evaluation, and no evidence of the reported failure was provided.
Event or Problem Description
Additional information the case was completed using a replacement ar-7268r radiopaque fibertape cerclage.There was no case delay and no additional anesthesia administered.

• Brand Name: RADIOPAQUE FIBERTAPE CERCLAGE W/O NEEDLE
• Common Device Name: POLYETHYLENE SYNTHETIC SUTURE
• Manufacturer (Section D): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• Manufacturer (Section G): ARTHREX, INC.; 1370 creekside boulevard; naples FL 34108 1945
• Manufacturer Contact: jared engle ; 8009337001
• MDR Report Key: 23475406
• Report Number: 1220246-2025-05001
• Device Sequence Number: 10499403
• Product Code: GAT
• UDI-Device Identifier: 00888867392021
• UDI-Public: (01)00888867392021(11)231110(17)281031(10)15165951R
• Combination Product (Y/N): N
• Initial Reporter State: AL
• Initial Reporter Country: US
• PMA/510(K) Number: K230976
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Distributor
• Initial Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial,Followup
• Report Date (Section B): 03/03/2026

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 Model Number: RADIOPAQUE FIBERTAPE CERCLAGE W/O NEEDLE
• Device Catalogue Number: AR-7268R
• Device Lot Number: 15165951R
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/27/2025
• Supplement Date Received by Manufacturer: 03/03/2026
• Initial Report FDA Received Date: 11/05/2025
• Supplement Report FDA Received Date: 03/03/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/10/2023
• 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 Sex: Unknown