DRILL BIT, 1.7MM
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
INVESTIGATION IS IN PROCESS. A FOLLOW-UP REPORT WILL BE PROVIDED UPON AVAILABILITY OF ADDITIONAL INFORMATION.
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.
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 |