Medical Device

Alphenix INFX-8000C/B5

Recall date: 2026-10-14 · Source: FDA_DEVICE

Brand / Firm

Product

Reason for recall

Loosening of the bolts securing the longitudinal movement mechanism may cause the tabletop to shift, resulting in [positional/imaging/patient] misalignment and a longitudinal motion error

Units affected

1 unit

Description

Alphenix INFX-8000C/B5

View official recall notice →