FDA Recall Open, Classified

Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray device produces conventional 2D X-ray images and Xray projection images for the reconstruction of a 3D view. The device is operated and used by qualified healthcare professionals.

Recall: Z-2413-2024 · Initiated October 28, 2021

Recall

Recall Number
Z-2413-2024
Event Number
95017
Firm
Palodex Group Oy Nahkelantie 160 Tuusula Finland
FEI Number
3005383085
Product Code
OAS
Status
Open, Classified
Root Cause
Radiation Control for Health and Safety Act
Initiated
October 28, 2021
Posted
August 12, 2024

Description

Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray device produces conventional 2D X-ray images and Xray projection images for the reconstruction of a 3D view. The device is operated and used by qualified healthcare professionals.

Reason

It was noticed in production on 28.10.2021, that the final testing database gives a pass result for Pan ADC repeatability test even when the test result is not within the set acceptance criteria (repeatability within 4%).

Action

Palodex Group Oy is preparing a Class IlIl field correction to update the firmware of ORTHOPANTOMOGRAPH OP 3D Pro of the 27 defective units and these devices will be retested for Pan ADC reproducibility. All affected persons will be notified of this defect in accordance with 21 CFR 806.10.

Distribution

US Nationwide-Worldwide

Quantity

103