FDA recall Z-3043-2026

Philips North America Llc · Class II · device

Product

Philips Brilliance CT 64: Brilliance CT 64 Channel Product Code: 728231, Brilliance CT 64 Upgrades Product Code: 728232. Software 4.1.10.x

Reason for recall

Philips has identified an unintended radiation issue with the Philips IQon, iCT, Ingenuity, and Brilliance CT 64 systems that could affect the performance of the equipment.

Distribution

US and US Territories.

Key facts

Status
Ongoing
Initiation date
2026-08-07
Report date
2026-09-09
Voluntary/Mandated
FDA Mandated
Location
Cambridge, MA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3043-2026