MAUDE Adverse Event Report: ARTHREX, INC. FIBERRING WITH SHUTTLE SUTURE25MM,SINGLE; POLYETHYLENE SYNTHETIC SUTURE

Model Number	FIBERRING WITH SHUTTLE SUTURE25MM,SINGLE
Medical Device Problem Code	Device Dislodged or Dislocated (2923)
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	05/01/2024
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The contribution of the device to the reported event could not be determined as the device was not returned for evaluation.The root cause of the event could not be determined from the information available and without device evaluation.If the device becomes available for evaluation, a follow-up report will be submitted.
Event or Problem Description
On 01 may 2024 it was reported by a product surveillance specialist in arthrex inc that they had received a report of a potential adverse event that occurred during a clinical study in the university of western australia.The arthrex products that were involved were: ar-1588r-ib acl repair tightrope, with internal brace, ar-2324pslc-1 peek swive lock c,4.75x19.1mm & ar-7282-25-1 fiberring with shuttle suture 25mm,single.It was reported that the patient experienced post-operative partial occlusion of peroneal vein, treated with eliquis with full recovery and without further sequalae.More information to be confirmed.There was case involvement.
Additional Manufacturer Narrative
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 a most likely cause.The most likely cause for the reported failure can be attributed to a patient-specific event.

• Brand Name: FIBERRING WITH SHUTTLE SUTURE25MM,SINGLE
• 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: 19562801
• Report Number: 1220246-2024-06016
• Device Sequence Number: 7575220
• Product Code: GAT
• UDI-Device Identifier: 00888867363694
• UDI-Public: 00888867363694
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K122374
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Study,Distributor
• Initial Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial,Followup
• Report Date (Section B): 09/13/2024

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 Model Number: FIBERRING WITH SHUTTLE SUTURE25MM,SINGLE
• Device Catalogue Number: AR-7282-25-1
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/01/2024
• Supplement Date Received by Manufacturer: 08/30/2024
• Initial Report FDA Received Date: 06/18/2024
• Supplement Report FDA Received Date: 09/13/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• 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 Sex: Unknown