MAUDE Adverse Event Report: PRECISION SPINE, INC REFORM PEDICLE SCREW SYSTEM; SCREWDRIVER

Catalog Number 39-RD-0060

Device Problem Fracture (1260)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Type  malfunction  

Manufacturer Narrative

H3 device evaluation - the driver was returned with a fracture of the tip.The fracture plane is skewed relative to the driver's longitudinal axis.This is indicative of parts failing under combination loading.It is believed that bending moments were applied in combination with torque which led to this failure.The part has likely seen extensive use since being fabricated in 2015 so this failure may have been initiated during prior usage.It is unclear if a counter torque wrench was being used during set screw tightening.Proper use of a counter torque wrench helps mitigate bending moments acting on the driver's tip.Review of device history records found fifteen (15) pieces of lot 0166it released for distribution on 1/19/2015 with no deviation or anomalies.Review of complaint history did not reveal a trend for reports of this nature for this part number.No corrective actions are being recommended.

Event Description

It was reported that the tip of the t25, lock-screw torque driver, reform (39-rd-0060) broke when it kicked out of the cap screw while torqueing a lock screw.The tip was recovered and the procedure completed utilizing other instrumentation readily available.There was no patient injury or delay to the procedure reported.

• Brand Name: REFORM PEDICLE SCREW SYSTEM
• Type of Device: SCREWDRIVER
• Manufacturer (Section D): PRECISION SPINE, INC; 2050 executive drive; pearl MS 39208
• Manufacturer (Section G): PRECISION SPINE, INC; 2050 executive drive; pearl MS 39208
• Manufacturer Contact: mike dawson ; 2050 executive drive; pearl, MS 39208 ; 6014204244
• MDR Report Key: 19023042
• MDR Text Key: 339207596
• Report Number: 3005739886-2024-00021
• Device Sequence Number: 1
• Product Code: HXX
• UDI-Device Identifier: 00840019928366
• UDI-Public: 00840019928366
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: EXEMPT
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Distributor
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 03/07/2024

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
• Device Operator: Health Professional
• Device Catalogue Number: 39-RD-0060
• Device Lot Number: 0166IT
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/11/2024
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 03/07/2024
• Initial Date FDA Received: 04/02/2024
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 01/19/2015
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1