MAUDE Adverse Event Report: MDT POWERED SURGICAL SOLUTIONS ENT MR8; MOTOR, DRILL, ELECTRIC

Model Number	1847DRLMTR
Medical Device Problem Code	Overheating of Device (1437)
Health Effect - Clinical Codes	Insufficient Information (4580); No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/16/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
H3 product analysis for product id 1847drlmtr, (b)(6): device returned, evaluation anticipated but not yet begun.Product id 1847attas, serial/lot #: (b)(6), serial/lot #: (b)(6): device is not yet returned to manufacturer.Continuation of d10: section d information references the main component of the system.Other relevant device(s) are: product id: 1847attas, serial/lot #: (b)(6), udi#: (b)(4); product id: 1847attss, serial/lot #: (b)(6), udi#: (b)(4).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.
Event or Problem Description
Repair request initiated for device with the report of overheating.No patient impact reported.
Additional Manufacturer Narrative
Product analysis :evaluation could not reproduce the reported malfunction of overheating as the temperature observed was 88 f.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.
Event or Problem Description
Repair request initiated for device with the report of overheating.It was reported that there was no patient involvement.
Additional Manufacturer Narrative
H3 product analysis: product id: 1847attas, serial/lot #: (b)(6), ubd, udi#: (b)(4), evaluation determined that device is overheating.The l ikely cause of the failure could not be determined.Product id: 1847attss, serial/lot #: (b)(6), ubd, udi#: (b)(4), evaluation could not reproduce the reported malfunction of overheating.Details of correction: 1.B5 updated 2.Ime code updated from e2401 to e2403 3.Imf code updated from f24 to f27 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: ENT MR8
• Common Device Name: MOTOR, DRILL, ELECTRIC
• 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: justin ellis ; 8200 coral sea street ne mvs21; mounds view, MN 55112 ; 7635265677
• MDR Report Key: 22847917
• Report Number: 1625507-2025-01952
• Device Sequence Number: 4419398
• Product Code: HBC
• UDI-Device Identifier: 00763000356958
• UDI-Public: (01)00763000356958(11)231101(20)02
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• PMA/510(K) Number: K183515
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 10/08/2025

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
• Operator of Device: Health Professional
• Device Model Number: 1847DRLMTR
• Device Catalogue Number: 1847DRLMTR
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/04/2025
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/30/2025
• Supplement Date Received by Manufacturer: 09/29/2025; 10/06/2025
• Initial Report FDA Received Date: 08/20/2025
• Supplement Report FDA Received Date: 10/07/2025; 10/08/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/01/2023
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown