Siemens Cios Care Fusion System Recall: Missing Insulating Foil Hazard

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Recalling firmSiemens Medical Solutions USA, Inc40 Liberty Blvd · Malvern, PA 19355-1418

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Siemens is recalling its Cios Care Fusion System (material #1030:8192, serial #31375) because the DAP chamber may be missing an insulating foil. This could lead to electrical issues if the system is used without proper insulation.

Why it’s dangerous

The DAP chamber may be missing an insulating foil, which could cause electrical short circuits or malfunctions if the system is used without proper insulation. This might lead to equipment failure during medical procedures.

Who’s affected

Healthcare facilities using the Siemens Cios Care Fusion System with material #10308192 and serial #31375 are affected. Medical staff and patients using the system are at risk if the insulating foil is missing.

How to tell if you have this one

Check for material number 10308192 and serial number 31375 on the Cios Care Fusion System. The product was sold by Siemens Medical Solutions USA, Inc.

Brand
Siemens
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify the material number 10308192 and serial number 31375 on your Cios Care Fusion System.

✎ GovInfoNow

Questions people ask

Is this recall affecting my medical equipment?

Yes, if your Cios Care Fusion System has material number 10308192 and serial number 31375.

What should I do if I have this product?

The recall does not specify a remedy, so check with Siemens Medical Solutions USA, Inc for further instructions.

Could this cause serious injury?

The recall states the DAP chamber may be missing an insulating foil, but no specific injury risk is mentioned.

Take action

Contact Siemens

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

✉️ Open in email

Subject: Recall Z-1954-2019 — Siemens Siemens

Hello,

I own a Siemens that is covered by recall Z-1954-2019 from Siemens.

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-1954-2019 (June 20, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1954-2019 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 Medical Solutions USA, Inc recalls Cios care fusion system

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