FDA Adverse Event Malfunction Summary report: N

DRILL BIT, 1.7MM

MDR report key: 19960673 · Received August 12, 2024

Report

Report Number
1220246-2024-07132
Event Type
Malfunction
Date Received
August 12, 2024
Date of Event
July 10, 2024
Report Date
September 23, 2024
Manufacturer
ARTHREX, INC.
Product Code
HTW
UDI-DI
00888867048942
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
501

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION IS IN PROCESS. A FOLLOW-UP REPORT WILL BE PROVIDED UPON AVAILABILITY OF ADDITIONAL INFORMATION.

Additional Manufacturer Narrative · 0

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 IMPROPER BONE PREP; MISALIGNED INSERTION; PRYING/LEVERAGING THE DEVICE DURING USE.

Description of Event or Problem · 0

ON 16 JULY 2024, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT BOTH AN AR-8916-14 DRILL BIT, 1.7MM AND AN AR-18700-54 DRIVER SHAFT, T8, SELF RETAINING, AO, BROKE DURING USE. THIS OCCURRED ON (B)(6) 2024 IN FLINDERS MEDICAL CENTRE DURING A NAVICULAR ORIF. USING ARTHREX EQUIPMENT FOR OPEN REDUCTION INTERNAL FIXATION 1.7MM DRILL BIT (REF: AR-8916-14) SNAPPED AT DRILL TIP. 2.4MM T8 SCREWDRIVER (REF: AR-18700-54) SNAPPED WHILE SCREWING LOCKING SCREW INTO LOCKING PLATE. AR-18724P-54 PLATE REMOVED FROM PATIENT AS SCREW THREAD SECURED INTO PLATE AND UNABLE TO BE REMOVED. ALL ARTHREX STOCK REMOVED AND DISCARDED. THE CASE WAS COMPLETED SUCCESSFULLY USING A SYNTHES VA FOOT SET. THERE WAS CASE INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2028223 DRILL BIT, 1.7MM DRILL BIT HTW ARTHREX, INC. DRILL BIT, 1.7MM 032338 00888867048942

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown