No image published for this recall

No image published for this recall

GE Medical GE SIGNA Voyager AIR (China Only), Nuclear Magnetic Resonance Imaging System - safety alert

Official notice

20 Aug 2025

Last checked

20 Aug 2025

Medium riskFDA

An official FDA notice concerns GE Medical GE SIGNA Voyager AIR (China Only), Nuclear Magnetic Resonance Imaging System - safety alert. An official FDA notice concerns GE SIGNA Voyager AIR (China Only), Nuclear Magnetic Resonance Imaging System. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2025-08-20. Recall numbers: Z-2311-2025. Check the official notice for the complete list. Published 2025-08-20.

What to do now

The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.

Recall number

Z-2311-2025

Official notice

2025-08-20

The hazard

An official FDA notice concerns GE SIGNA Voyager AIR (China Only), Nuclear Magnetic Resonance Imaging System. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2025-08-20. Recall numbers: Z-2311-2025. Check the official notice for the complete list.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Event Ids

97187

Recall Numbers

Z-2311-2025

Checked manually this time?

The app alerts you when a new official recall is published — no searching, no checking back.

Turn on recall alerts

Affected products

Product 1

GE SIGNA Voyager AIR (China Only), Nuclear Magnetic Resonance Imaging System

Risk / hazard

An official FDA notice concerns GE SIGNA Voyager AIR (China Only), Nuclear Magnetic Resonance Imaging System. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2025-08-20. Recall numbers: Z-2311-2025. Check the official notice for the complete list.

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States · WI · Waukesha

Affected area 1

US · United States · WI · Waukesha

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: GE Medical. Contact: GE Medical Systems, LLC.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-2311-2025

Event id

97187

Status

active

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
Something wrong on this page?

Related recalls

US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA3 Sept 2025
US
No image published for this recall

SIGNA Architect - safety alert

Medium riskFDA30 Jul 2025
US
No image published for this recall

GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed - safety alert

High riskFDA19 Mar 2025
US
No image published for this recall

a product listed in the official notice - safety alert

High riskFDA23 Apr 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA17 Dec 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA18 Jun 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA29 Oct 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA22 Oct 2025
US
No image published for this recall

GE Healthcare Optima XR200amx, Mobile Digital Radiographic System, Model Numbers: 1) 5555000-3; 2) 5555000-4: 3) A0659MB - safety alert

Medium riskFDA15 Jan 2025
US
No image published for this recall

a product listed in the official notice - safety alert

Medium riskFDA14 Aug 2024
US
No image published for this recall

B105P Patient Monitor (with E-module slot option), REF 6160000-001-XXXXXX, - safety alert

Medium riskFDA28 Dec 2022
US
No image published for this recall

a product listed in the official notice - safety alert

Critical riskFDA31 Oct 2018

Weekly recall digest

Get next week's recalls before you need them.

One email every Monday — official-source recalls for your country, and nothing else. Unsubscribe from any email.

The digest is the slow lane — one email a week. For instant, severity-gated alerts the moment a notice is published, get the app.

This recall was published 20 Aug 2025. The next one won't wait for you to search.

RecallScope watches official sources for the brands and VINs you follow, and alerts you the moment a new notice is published.