MAUDE Adverse Event Report: ARTHREX, INC. C-MOUNT AR-SCOPE,30°2.7X 72MM LGTH; ARTHROSCOPE AND ACCESSORIES

Model Number	C-MOUNT AR-SCOPE,30°2.7X 72MM LGTH
Medical Device Problem Code	Crack (1135)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/30/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Investigation is in process.A follow-up report will be provided upon availability of additional information.
Event or Problem Description
On 07/30/2024, it was reported by a sales representative via (b)(4) that an ar-3355-2730 scope is damaged.A doctor was attempting to do an ankle scope and hit the scope with a burr.The scope is now cracked.This occurred during use in a case with no patient effect.Another device was used to complete the case.
Additional Manufacturer Narrative
Additional information: d9, g3, h3, h6.The most likely cause for the reported failure can be attributed to misuse/mishandling due to damage to the device.

• Brand Name: C-MOUNT AR-SCOPE,30°2.7X 72MM LGTH
• Common Device Name: ARTHROSCOPE AND ACCESSORIES
• 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: 20038635
• Report Number: 1220246-2024-07234
• Device Sequence Number: 11512688
• Product Code: HRX
• UDI-Device Identifier: 00888867029835
• UDI-Public: 00888867029835
• Combination Product (Y/N): N
• Initial Reporter State: GA
• Initial Reporter Country: US
• PMA/510(K) Number: K080560
• 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): 02/14/2025

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: C-MOUNT AR-SCOPE,30°2.7X 72MM LGTH
• Device Catalogue Number: AR-3355-2730
• Device Lot Number: 15027258
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/30/2024
• Supplement Date Received by Manufacturer: 01/28/2025
• Initial Report FDA Received Date: 08/22/2024
• Supplement Report FDA Received Date: 02/14/2025
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown