MIDAS REX LEGEND
Report
- Report Number
- 1625507-2025-00299
- Event Type
- Malfunction
- Date Received
- February 18, 2025
- Date of Event
- April 4, 2023
- Report Date
- February 16, 2025
- Manufacturer
- MDT POWERED SURGICAL SOLUTIONS
- Product Code
- HBB
- UDI-DI
- 00613994418821
- PMA / PMN Number
- K020069
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
H3: PRODUCT ANALYSIS: EVALUATION DETERMINE THAT THE DEVICE WAS TESTED AND THE TEMPERATURE WAS MEASURED TO BE 112.3 DEGREES FAHRENHEIT. HOWEVER, THE RATE OF TEMPERATURE RISE WAS BELOW THRESHOLD. THE LIKELY CAUSE WAS IDENTIFIED AS BEARING CORRODED. IT WAS ALSO NOTED BEARING IS WORN, THE DEVICE MAKES NOISE. THIS REGULATORY REPORT IS BEING SUBMITTED DUE TO A 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.
REPAIR REQUEST INITIATED FOR DEVICE WITH THE REPORT OF OVERHEATING. IT WAS REPORTED THAT THERE WAS NO PATIENT INVOLVEMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1208627 | MIDAS REX LEGEND | MOTOR, DRILL, PNEUMATIC | HBB | MDT POWERED SURGICAL SOLUTIONS | AA10S | 00613994418821 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |