FDA Device recall Z-2598-2025

Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306

FDA Device
Class II
ongoing
Published 2025-10-01

On 2025-10-01 the FDA classified a Class II recall of Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306 by Philips North America, citing the patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2598-2025
Classification	Class II
Status	ongoing
Initiated	2025-08-13
Published	2025-10-01
Last updated	2026-09-13 11:57 UTC
Company	Philips North America
Distribution	US

Product

Philips CT systems labeled as the following: 1. Brilliance iCT, Model Number: 728306.

Reason

The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

Identifiers

code_info	1. Model Number: 728306; UDI-DI: 00884838059474; Serial Number: 100068, 100188, 100241, 100288, 100332, 100365, 100461,… 1. Model Number: 728306; UDI-DI: 00884838059474; Serial Number: 100068, 100188, 100241, 100288, 100332, 100365, 100461, 85007, 85016, 100657, 100682, 100686, 100779, 100832, 100783, 100775, 100788, 100807, 100828, 100816, 85136, 85153, 100043, 100038, 100082, 100074, 100081, 100097, 100098, 100119, 100111, 100113, 100123, 100130, 100133, 100222, 100141, 100134, 100160, 100157, 100150, 100158, 100180, 100161, 100173, 100215, 100064, 100117, 100247, 100172, 100196, 200045, 100191, 100374, 100189, 100230, 100203, 100201, 100204, 100211, 100234, 100227, 100249, 100285, 100245, 100253, 100226, 100264, 100292, 100268, 100294, 100302, 100315, 100301, 100310, 100336, 100314, 100349, 100354, 100321, 100389, 100385, 100446, 100424, 100401, 100352, 100404, 100511, 100412, 100438, 100435, 100455, 100380, 100487, 100429, 100427, 100443, 100393, 100413, 100462, 100604, 100456, 100497, 100498, 100502, 100500, 100445, 100510, 100505, 100513, 100635, 85018, 85014, 100612, 85041, 100603, 85035, 85028, 1

code_info

1. Model Number: 728306; UDI-DI: 00884838059474; Serial Number: 100068, 100188, 100241, 100288, 100332, 100365, 100461,…

1. Model Number: 728306; UDI-DI: 00884838059474; Serial Number: 100068, 100188, 100241, 100288, 100332, 100365, 100461, 85007, 85016, 100657, 100682, 100686, 100779, 100832, 100783, 100775, 100788, 100807, 100828, 100816, 85136, 85153, 100043, 100038, 100082, 100074, 100081, 100097, 100098, 100119, 100111, 100113, 100123, 100130, 100133, 100222, 100141, 100134, 100160, 100157, 100150, 100158, 100180, 100161, 100173, 100215, 100064, 100117, 100247, 100172, 100196, 200045, 100191, 100374, 100189, 100230, 100203, 100201, 100204, 100211, 100234, 100227, 100249, 100285, 100245, 100253, 100226, 100264, 100292, 100268, 100294, 100302, 100315, 100301, 100310, 100336, 100314, 100349, 100354, 100321, 100389, 100385, 100446, 100424, 100401, 100352, 100404, 100511, 100412, 100438, 100435, 100455, 100380, 100487, 100429, 100427, 100443, 100393, 100413, 100462, 100604, 100456, 100497, 100498, 100502, 100500, 100445, 100510, 100505, 100513, 100635, 85018, 85014, 100612, 85041, 100603, 85035, 85028, 1

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2598-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.