MAUDE Adverse Event Report: ARTHREX, INC. EASY-OUT, LARGE COMPRESSION FT; ORTHOPEDIC MANUAL SURG INSTR

Model Number	EASY-OUT, LARGE COMPRESSION FT
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/22/2026
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
It was reported that during a removal of osteosynthesis material, the screw remover fractured during screw extraction.Per complaint reporter there was no harm for patient, operator or third party.The surgery was finished successfully with a different screwdriver.It was not necessary to switch the surgical technique or do a second surgery.
Additional Manufacturer Narrative
Additional information: d9, g3, h3, h6 the reported event was confirmed as one unpackaged ar-8750-10, easy-out, large compression ft, batch number 1391932, was received for investigation.Upon visual inspection, it was observed that the tip is broken off (see evaluation picture 3).Functional testing was not performed due to the damage of the device.No fragments were returned for evaluation.A most likely cause is attributed to wear and tear considering the age of the device (manufacturing year 2019).

• Brand Name: EASY-OUT, LARGE COMPRESSION FT
• Common Device Name: ORTHOPEDIC MANUAL SURG INSTR
• 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: 25135286
• Report Number: 1220246-2026-02764
• Device Sequence Number: 21163528
• Product Code: LXH
• UDI-Device Identifier: 00888867263611
• UDI-Public: (01)00888867263611(11)190813(10)1391932
• Combination Product (Y/N): N
• Initial Reporter Country: SP
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Company Representative
• Initial Reporter Occupation: Administrator/Supervisor
• Type of Report: Initial,Followup
• Report Date (Section B): 07/01/2026

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: EASY-OUT, LARGE COMPRESSION FT
• Device Catalogue Number: AR-8750-10
• Device Lot Number: 1391932
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/23/2026
• Supplement Date Received by Manufacturer: 06/23/2026
• Initial Report FDA Received Date: 05/11/2026
• Supplement Report FDA Received Date: 07/01/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 08/13/2019
• 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