Siemens APTIO 900: Pacemaker Interference Risk Recall

Take action

Contact the company & request your remedy

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 9000 refrigerated storage modules that may have been shipped without a warning label for potential interference with pacemaker function. This could pose a risk to individuals with pacemakers.

Why it’s dangerous

The refrigerated storage modules may lack a warning label that could interfere with pacemaker function. This interference might cause unintended pacemaker behavior, potentially affecting health.

Who’s affected

People with pacemakers who use the APTIO 9000 refrigerated storage modules are most at risk. The recall affects specific Siemens Healthcare product models.

How to tell if you have this one

Check for Siemens Healthcare APTIO 9000 refrigerated storage modules with material numbers 10703049 or 10715227. The recall covers units sold with UDI 00630414594477.

Brand
Siemens Healthcare
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check for Warning Label
Look for a warning label indicating potential pacemaker interference on the module.

✎ GovInfoNow

Questions people ask

Do I need to stop using this product?

The recall does not require immediate stop use; check for the warning label first.

What is the specific model number for this recall?

The specific model numbers are 10703049 and 10715227.

How can I confirm if my unit is affected?

Check the unit's material numbers (10703049 or 10715227) or UDI (00630414594477).

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-0213-2019 — Siemens Healthcare Siemens Healthcare

Hello,

I own a Siemens Healthcare that is covered by recall Z-0213-2019 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-0213-2019 (August 14, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0213-2019 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 9000 REFRIGERATED STORAGE MODULE

Use caution until it’s fixed