FDA Adverse Event Malfunction Summary report: N

MIDAS REX MR8

MDR report key: 21641599 · Received March 19, 2025

Report

Report Number
1625507-2025-00933
Event Type
Malfunction
Date Received
March 19, 2025
Date of Event
March 4, 2024
Report Date
March 19, 2025
Manufacturer
MDT POWERED SURGICAL SOLUTIONS
Product Code
HBB
UDI-DI
00643169912373
PMA / PMN Number
K183515
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

H3: PRODUCT ANALYSIS: EVALUATION COULD NOT BE PERFORMED BECAUSE BEARINGS ARE BROKEN AND CORRODED. IT WAS NOTED THAT THERE WAS DIFFICULT TO INSERT TOOL INTO THE ATTACHMENT. THIS FINDING MAY HAVE CONTRIBUTED TO THE USER'S EXPERIENCE. IT WAS ALSO NOTED THAT THERE WAS LOCK TWIST JAMMED AND OUTPUT DRIVE SHAFT ASSEMBLY CORRODED.. THIS REGULATORY REPORT IS BEING SUBMITTED DUE TO RETROSPECTIVE REVIEW THROUGH CAPA 624392. 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.

Description of Event or Problem · 0

REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. IT WAS REPORTED THERE WAS NO PATIENT INVOLVEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
547383 MIDAS REX MR8 MOTOR, DRILL, PNEUMATIC HBB MDT POWERED SURGICAL SOLUTIONS MR8-AA14 00643169912373

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown