Siemens APTIO RACK INPUT MODULE Recall: Pacemaker Interference Risk

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Siemens Healthcare is recalling APTIO R: Rack Input Modules that may lack a warning label for pacemaker interference. This could cause pacemaker malfunction if the device is not properly labeled.

Why it’s dangerous

The modules may have been shipped without a warning label that could interfere with pacemaker functionality. This risk exists if the module is not properly labeled, potentially causing pacemaker malfunction.

Who’s affected

Users of medical devices with pacemakers who install or use these modules without proper labeling. Those with pacemakers are at risk if the module is not labeled correctly.

How to tell if you have this one

Check for Siemens Material Numbers 10703037 or 10711144 on the APTIO RACK INPUT MODULE. The unique device identifier (UDI) 00630414594477 may also be present.

Brand
Siemens Healthcare
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Labeling
Verify if the module has a warning label for pacemaker interference.

✎ GovInfoNow

Questions people ask

What is the specific model number for this recall?

The specific material numbers are 10703037 and 10711144.

How can I tell if my module is affected?

Check for Siemens Material Numbers 10703037 or 10711144 on the APTIO RACK INPUT MODULE.

Do I need to stop using this module?

The recall does not require stopping use; check for a warning label to ensure pacemaker safety.

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-0210-2019 — Siemens Healthcare Siemens Healthcare

Hello,

I own a Siemens Healthcare that is covered by recall Z-0210-2019 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-0210-2019 (August 14, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0210-2019 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 APTIO RACK INPUT MODULE

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