FDA recall Z-2413-2024

Palodex Group Oy · Class II · device

Product

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 for recall

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%).

Distribution

US Nationwide-Worldwide

Key facts

Status
Ongoing
Initiation date
2021-10-28
Report date
2024-08-21
Voluntary/Mandated
FDA Mandated
Location
Tuusula, Finland

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2413-2024