MAUDE Adverse Event Report: MDT POWERED SURGICAL SOLUTIONS MOTOR ENT MR8 ELECTRIC; DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE

Model Number 1847DRLMTR

Device Problem Overheating of Device (1437)

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

Event Type  malfunction  

Event Description

Repair request initiated for device with the report of overheating.No patient impact reported.Repair is being escalated to product event due to reason for the return.

Manufacturer Narrative

H3: evaluation determined that the device was tested and the maximum temperature was measured to be 138 degrees fahrenheit.The likely cause of failure could not be determined.It was also noted that the rotor housing was loose and the rotor shaft was cracked.Date of notification: 2024-feb-09 medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.

• Brand Name: MOTOR ENT MR8 ELECTRIC
• Type of Device: DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE
• Manufacturer (Section D): MDT POWERED SURGICAL SOLUTIONS; 4620 n beach st; fort worth TX 76137
• Manufacturer (Section G): MDT POWERED SURGICAL SOLUTIONS; 4620 n beach st; fort worth TX 76137
• Manufacturer Contact: glen belmer ; 7000 central avenue ne; ft. worth, TX 76137-3291 ; 6122713209
• MDR Report Key: 18977166
• MDR Text Key: 338554571
• Report Number: 1625507-2024-00096
• Device Sequence Number: 1
• Product Code: HBE
• UDI-Device Identifier: 00763000356958
• UDI-Public: 00763000356958
• Combination Product (y/n): N
• Reporter Country Code: SP
• PMA/PMN Number: K183515
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Health Professional,Company Representative
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 03/26/2024

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 Model Number: 1847DRLMTR
• Device Catalogue Number: 1847DRLMTR
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 02/16/2024
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 02/28/2024
• Initial Date FDA Received: 03/26/2024
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 05/03/2021
• 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