FDA Device recall Z-1567-2024

Ingenia 3.0T CX, Magnetic Resonance System

FDA Device
Class II
ongoing
Published 2024-04-24

On 2024-04-24 the FDA classified a Class II recall of Ingenia 3.0T CX, Magnetic Resonance System by Philips North America, citing patient support table floor plate may be incorrectly installed.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1567-2024
Classification	Class II
Status	ongoing
Initiated	2024-03-12
Published	2024-04-24
Last updated	2026-09-13 11:57 UTC
Company	Philips North America
Distribution	US

Product

Ingenia 3.0T CX, Magnetic Resonance System.

Reason

Patient support table floor plate may be incorrectly installed.

Identifiers

code_info	Model No. 781271, 782105; UDI-DI 884838068452, 884838098312; Serial No. 78000, 78003, 78004, 78005, 78007, 78035, 78062… Model No. 781271, 782105; UDI-DI 884838068452, 884838098312; Serial No. 78000, 78003, 78004, 78005, 78007, 78035, 78062, 78010, 78009, 78011, 78012, 78014, 78013, 78015, 78016, 78017, 78018, 78025, 78021, 78019, 78023, 78043, 78068, 78026, 78053, 78027, 78028, 78039, 78029, 78030, 78031, 78032, 78033, 78034, 78036, 78038, 78040, 78070, 78042, 78044, 78045, 78082, 78046, 78047, 78048, 78049, 78051, 78115, 78050, 78008, 78058, 78059, 78060, 78063, 78064, 78065, 78067, 78066, 78071, 78072, 78073, 78074, 78075, 78076, 78077, 78078, 78080, 78081, 78083, 78084, 78086, 78087, 78088, 78089, 78091, 78092, 78094, 78095, 78101, 78096, 78097, 78099, 78098, 78100, 78102, 78113, 78114, 78109, 78103, 78104, 78106, 78107, 78110, 78117, 78112, 78118, 78111, 78120, 78129, 78121, 78122, 78123, 78126, 78127, 78128, 78132, 78133, 78135, 78138, 78137, 78139, 78140, 78141, 78142, 78145, 78149, 78147, 78148, 78150, 78151, 78154, 78155, 78156, 78158, 78162, 78164, 78166, 78167, 78157, 78171, 78173, 78172, 7817

code_info

Model No. 781271, 782105; UDI-DI 884838068452, 884838098312; Serial No. 78000, 78003, 78004, 78005, 78007, 78035, 78062…

Model No. 781271, 782105; UDI-DI 884838068452, 884838098312; Serial No. 78000, 78003, 78004, 78005, 78007, 78035, 78062, 78010, 78009, 78011, 78012, 78014, 78013, 78015, 78016, 78017, 78018, 78025, 78021, 78019, 78023, 78043, 78068, 78026, 78053, 78027, 78028, 78039, 78029, 78030, 78031, 78032, 78033, 78034, 78036, 78038, 78040, 78070, 78042, 78044, 78045, 78082, 78046, 78047, 78048, 78049, 78051, 78115, 78050, 78008, 78058, 78059, 78060, 78063, 78064, 78065, 78067, 78066, 78071, 78072, 78073, 78074, 78075, 78076, 78077, 78078, 78080, 78081, 78083, 78084, 78086, 78087, 78088, 78089, 78091, 78092, 78094, 78095, 78101, 78096, 78097, 78099, 78098, 78100, 78102, 78113, 78114, 78109, 78103, 78104, 78106, 78107, 78110, 78117, 78112, 78118, 78111, 78120, 78129, 78121, 78122, 78123, 78126, 78127, 78128, 78132, 78133, 78135, 78138, 78137, 78139, 78140, 78141, 78142, 78145, 78149, 78147, 78148, 78150, 78151, 78154, 78155, 78156, 78158, 78162, 78164, 78166, 78167, 78157, 78171, 78173, 78172, 7817

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-1567-2024%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.