FDA Adverse Event Malfunction Summary report: N

ROSA ONE

MDR report key: 8072890 · Received November 15, 2018

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

Additional Manufacturer Narrative · 0

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).

Description of Event or Problem · 0

IT WAS REPORTED THAT DURING THE REGISTRATION STEP OF A SURGERY, FOUR 3D-REGISTRATION FAILURES OCCURRED.

Additional Manufacturer Narrative · 1

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.

Description of Event or Problem · 1

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