FDA Adverse Event Malfunction Summary report: N

ANGLED REAMER, DRIVE SHAFT

MDR report key: 19590371 · Received June 21, 2024

Report

Report Number
1220246-2024-06357
Event Type
Malfunction
Date Received
June 21, 2024
Date of Event
May 28, 2024
Report Date
September 19, 2024
Manufacturer
ARTHREX, INC.
Product Code
LXH
UDI-DI
00888867324954
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
501

Narratives

Additional Manufacturer Narrative · 0

THE COMPLAINT ALLEGATION IS CONFIRMED. ONE UNPACKAGED AR-9676, BATCH 022239, WAS RECEIVED FOR INVESTIGATION. THE VISUAL EVALUATION REVEALED HEAVY SCRATCHES AND LINES IN THE OUTSIDE DIAMETER AND SCRATCHES ALONG THE SHAFT. BOTH DEVICES ARRIVED SEPARATELY FOR INVESTIGATION. THE OBSERVED CONDITION IS MOST LIKELY DUE TO HEAVY USE. DURING THE FUNCTIONAL TESTING WITH THE AR-9597-20 PART FROM BATCH 37222223, RESISTANCE WAS ENCOUNTERED WHEN TRYING TO INSERT THE AR-9676. THE OBSERVED CONDITION IS MOST LIKELY CAUSED BY OVERHEATING DURING USE, WHICH CAN BE ATTRIBUTED TO THE AGE OR EXTENSIVE USE OF THE DEVICE.

Additional Manufacturer Narrative · 0

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.

Description of Event or Problem · 0

ON 05/28/2024, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA (B)(4) THAT AN AR-9676 ANGLED REAMERWAS OFF ANGLE AND CAUGHT THE INSIDE OF THE AR-9597-20 ANGLED REAMER SLEEVE AND BENT IT. THIS OCCURRED DURING A CASE WITH NO EFFECT ON THE PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1103209 ANGLED REAMER, DRIVE SHAFT MANUAL INSTR, GENERAL SURGICAL LXH ARTHREX, INC. ANGLED REAMER, DRIVE SHAFT 022239 00888867324954

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown