ROSA ONE
Report
- Report Number
- 3009185973-2018-00302
- Event Type
- Malfunction
- Date Received
- November 15, 2018
- Date of Event
- June 21, 2018
- Report Date
- November 28, 2018
- Manufacturer
- MEDTECH SA
- Product Code
- OLO
- PMA / PMN Number
- N/A
- Removal / Correction Number
- N/A
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AS
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
IT WAS REPORTED THAT THERE WERE FOUR 3D-REGISTRATION FAILURES. THE RECHNICAL INVESTIGATION CONFIRMED THAT THE 3D-REGISTRATION FAILED FOUR CONSECUTIVE TIMES DUE TO THE DISTURBANCE OF THE OPTICAL PATIENT REFERENCE BY THE 3D X-RAY PATTERN FRAME, WHICH IS A KNOWN DESIGN DEFECT. EVENT SUMMARY, DEVICE HISTORY RECORD REVIEW AND COMPLAINT HISTORY REVIEW DID NOT IDENTIFY CONTRIBUTING FACTORS. TWO PREVIOUS COMPLAINTS WERE RECEIVED FOR THIS DEVICE DUE TO THE SAME ROOT CAUSE. (B)(4). DATE RECEIVED BY MANUFACTURER (INVESTIGATION COMPLETION).
IT WAS REPORTED THAT DURING THE REGISTRATION STEP OF A SURGERY, FOUR 3D-REGISTRATION FAILURES OCCURRED.
THE DEVICE HAS NOT BEEN EVALUATED YET FOR INVESTIGATION PURPOSE. ONCE THE EVALUATION IS PERFORMED, A FOLLOW-UP MEDWATCH REPORT WILL BE SUBMITTED. THE DEVICE MODEL ROSA ONE IS NOT FDA CLEARED BUT IS SIMILAR TO THE DEVICE ROSA BRAIN, CLASSIFIED HAW AND CLEARED UNDER K172444.
IT WAS REPORTED THAT DURING THE REGISTRATION STEP OF A SURGERY, FOUR 3D-REGISTRATION FAILURES OCCURRED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 914851 | ROSA ONE | COMPUTER-ASSISTED SURGICAL DEVICE | OLO | MEDTECH SA | ROSA ONE | 3.1.0.1276 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |