The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer...

Philips North America Llc began a recall of The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into cross-sectional images of the body taken at... on 2022-03-29. FDA classified it as Class II and gives the reason as "Three software issues affecting incorrect image display, error interpreting patient images due to image reporting, and patient exposure to incorrect image/function during clinical use". As of 2026-09-10, the recall status on record is Completed, and MDM tags the root cause as software.