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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Arthrex, Inc. 2.4mm Cannulated Drill and Passing Wire; ORTHOPEDIC MANUAL SURG INSTR

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Arthrex, Inc. 2.4mm Cannulated Drill and Passing Wire; ORTHOPEDIC MANUAL SURG INSTR Back to Search Results
Model Number 2.4mm Cannulated Drill and Passing Wire
Medical Device Problem Code Break (1069)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/27/2026
Type of Reportable Event Malfunction
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Brand Name
2.4mm Cannulated Drill and Passing Wire
Common Device Name
ORTHOPEDIC MANUAL SURG INSTR
Manufacturer (Section D)
Arthrex, Inc.
1370 creekside boulevard
naples FL 34108 -194
Manufacturer (Section G)
Arthrex, Inc.
1370 creekside boulevard
naples FL 34108 -194
Manufacturer Contact
jared engle
+1(800)933-7001
MDR Report Key50715477
Report Number1220246-2026-04664
Device Sequence Number10598798
Product Code LXH
UDI-Device Identifier00888867365896
Combination Product (Y/N)N
Initial Reporter StateWI
Initial Reporter CountryUS
PMA/510(K) Number
EXEMPT
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Distributor
Initial Reporter Occupation Administrator/Supervisor
Type of Report Initial
Report Date (Section B) 09/10/2026
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 Number2.4mm Cannulated Drill and Passing Wire
Device Catalogue NumberAR-1594D-24
Device Lot Number15651414
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/27/2026
Initial Report FDA Received Date09/10/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Date Device Manufactured07/08/2026
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 Number1
Patient SexUnknown
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