GE Healthcare Discovery MR750 3.0T MRI System May Have Missing Anatomy in 3D Images

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Recalling firmGE Healthcare, LLC3000 N Grandview Blvd, N/A · Waukesha, WI 53188-1615

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✎ GovInfoNow plain-language explainer

What happened, in plain English

GE Healthcare is recalling some Discovery MR750 3.0T MRI systems because software issues might cause gaps in 3D images. This could lead to incomplete scans that affect diagnosis accuracy.

Why it’s dangerous

The software issue can cause missing slices in 3D volume images, creating gaps in anatomical structures. This might result in incomplete scans that could affect diagnostic accuracy, but the risk is not immediate or life-threatening.

Who’s affected

Medical facilities using GE's Discovery MR750 3.0T MRI systems with software version DV29.1 are affected. Patients undergoing scans on these systems may see incomplete images.

How to tell if you have this one

Check if your MRI system has the software version DV29.1. The product is a Discovery MR750 3.0T nuclear magnetic resonance imaging system.

Brand
GE Healthcare
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Software Version
Verify your MRI system's software version is DV29.1 to determine if it's affected.

✎ GovInfoNow

Questions people ask

Is this recall dangerous?

The recall is for potential missing anatomy in 3D images, which could affect scan accuracy but is not immediately dangerous.

How can I check if my MRI system is affected?

Check if your Discovery MR750 3.0T system has software version DV29.1.

What should I do if my system is affected?

The official recall does not specify a remedy, so contact GE Healthcare for further instructions.

Take action

Contact GE Healthcare

We’ve drafted a message you can send GE Healthcare to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0136-2022 — GE Healthcare GE Healthcare

Hello,

I own a GE Healthcare that is covered by recall Z-0136-2022 from GE Healthcare.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0136-2022 (August 26, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0136-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

GE Healthcare, LLC recalls Discovery MR750 3.0T nuclear magnetic resonance imaging system

Lower-risk recall