Siemens Atellica IM 130: Software Update Needed for Safety

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Contact the company & request your remedy

Recalling firmSiemens Healthcare Diagnostics, Inc.511 Benedict Ave, N/A · Tarrytown, NY 10591-5005

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Siemens Healthcare is recalling Atellica IM 1300 Analyzers with Material Number 11066001 because of software issues that need an update. This recall is important to prevent potential malfunctions in the device.

Why it’s dangerous

The system software has multiple issues that require an update. These issues could lead to potential malfunctions in the device if not addressed.

Who’s affected

Users of the Atellica IM 1300 Analyzer with Material Number 11066001 are affected. Laboratory staff and healthcare professionals using this device are most at risk.

How to tell if you have this one

Check for the Material Number 11066001 on the Atellica IM 1300 Analyzer. The device also has a Unique Device Identification (UDI) number starting with 00630414007960.

Brand
Siemens Healthcare
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Software Version
Verify the software version on your Atellica IM 1300 Analyzer to confirm if an update is needed.

✎ GovInfoNow

Questions people ask

Is this recall dangerous?

The recall is for software issues that require an update to prevent potential malfunctions, but it does not indicate a risk of serious injury.

How do I know if my Atellica IM 1300 Analyzer is affected?

Your device is affected if it has Material Number 11066001 or the Unique Device Identification (UDI) number starting with 00630414007960.

What should I do if my device is affected?

Check the software version to see if an update is needed. Siemens Healthcare will provide instructions for the update.

Take action

Contact Siemens Healthcare

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

✉️ Open in email

Subject: Recall Z-1299-2019 — Siemens Healthcare Siemens Healthcare

Hello,

I own a Siemens Healthcare that is covered by recall Z-1299-2019 from Siemens 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-1299-2019 (March 7, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1299-2019 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.

Siemens Healthcare Diagnostics, Inc. recalls Atellica IM 1300 Analyzer, Material Number 11066001

Lower-risk recall