GE Discovery NM/CT 670 CZT Recall: Possible Detector Mounting Failure

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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 certain Discovery NM/CT 670 CZT nuclear medicine imaging systems because improper installation may cause detector mounting failures. This could impact the safety of medical imaging procedures if not corrected.

Why it’s dangerous

During installation, some detector screws may not be secured properly, which could lead to loss of one detector mounting design redundancy. This might affect the system's ability to safely perform nuclear medicine imaging procedures.

Who’s affected

Healthcare facilities using the specific model codes listed in the recall. Medical staff and patients using these systems are at risk if the detector mounting issue remains unaddressed.

How to tell if you have this one

Check for model code H3906CT and specific system IDs listed: AD7X38019, AD7X38022, AD7X38020. These systems were sold with certain lot numbers between 2023 and 2024.

Brand
GE Healthcare
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check System ID
Verify your system's ID against the listed codes: AD7X38019, AD7X38022, or AD7X38020.

✎ GovInfoNow

Questions people ask

What is the model code for the recalled system?

The model code is H3906CT.

How can I tell if my system is affected?

Check for system IDs: AD7X38019, AD7X38022, or AD7X38020.

Is there a fix for this issue?

The recall record does not mention a remedy or fix.

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-1258-2019 — GE Healthcare GE Healthcare

Hello,

I own a GE Healthcare that is covered by recall Z-1258-2019 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-1258-2019 (March 20, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1258-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 20, 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 NM/CT 670 CZT, Model/Catalogue/Code H3906CT Product Usage: The GE Discovery NM/CT 670 CZT system is intended

Lower-risk recall