MIDAS REX LEGEND
Report
- Report Number
- 1625507-2025-00287
- Event Type
- Malfunction
- Date Received
- February 14, 2025
- Report Date
- February 14, 2025
- Manufacturer
- MDT POWERED SURGICAL SOLUTIONS
- Product Code
- HBB
- PMA / PMN Number
- K020069
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IT
- Reporter Occupation
- 003
Narratives
H3: PRODUCT ANALYSIS: EVALUATION COULD NOT BE PERFORMED BECAUSE SEIZED. IT WAS NOTED THAT WORN BEARINGS. THIS FINDING MAY HAVE CONTRIBUTED TO THE USER'S EXPERIENCE. IT WAS ALSO NOTED DEVICE HAS MINOR SCRATCHES. B3: DATE OF NOTIFICATION: 2023-01-11 (DATE OF EVENT OR ESTIMATED DATE OF INCIDENT NOT PROVIDED TO MANUFACTURER) 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 AND NOT SPINNING. NO PATIENT IMPACT REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1638331 | MIDAS REX LEGEND | MOTOR, DRILL, PNEUMATIC | HBB | MDT POWERED SURGICAL SOLUTIONS | AA10 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |