Siemens ADVIA 120/2120/2120i 3-in-1 TESTpoint Control recall: Incorrect platelet values

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Contact the company & request your remedy

Recalling firmSiemens Healthcare Diagnostics, Inc.511 Benedict Ave · 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 ADVIA 120/2120/2120i 3-in-1 TESTpoint Control units because they have incorrect platelet (PLT) value assignments. This could lead to inaccurate blood test results if the device is used without correction.

Why it’s dangerous

The device assigns the wrong platelet values, which could cause inaccurate blood test results. This might lead to incorrect medical decisions if the test results are used without correction.

Who’s affected

Users of the ADVIA 120/2120/2120i hematology systems who have the specific model with incorrect platelet value assignments are affected. Laboratory technicians and healthcare providers using these devices are most at risk.

How to tell if you have this one

Check for the Siemens Material Number 10330063 and lot numbers TP251035 or TP251045 on the device. The unique device identifier (UDI) 00630414473406 is also associated with affected units.

Brand
Siemens Healthcare
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Details
Look for the Siemens Material Number 10330063 and lot numbers TP251035 or TP251045 on the device.

✎ GovInfoNow

Questions people ask

What is the specific model of the device being recalled?

The recalled device is the ADVIA 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control).

What is the material number for the affected units?

The Siemens Material Number for affected units is 10330063.

What lot numbers are affected?

Lot numbers TP251035 and TP251045 are affected.

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-2087-2025 — Siemens Healthcare Siemens Healthcare

Hello,

I own a Siemens Healthcare that is covered by recall Z-2087-2025 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-2087-2025 (June 4, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2087-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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 ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control)

Lower-risk recall