Qiagen QIAamp DSP Virus Kit Recall: Decreased Performance Risk

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Contact the company & request your remedy

Recalling firmQiagen, GmbHQiagen Str. 1 · Hilden, N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Qiagen is recalling specific lots of the QIAamp DSP Virus Kit (Cat. No. 60704) because they may cause decreased performance in laboratory analytic workflows. This recall affects users who have these specific lot numbers and could impact the accuracy of their testing results.

Why it’s dangerous

The recalled lots of the QIAamp DSP Virus Kit may not perform as expected in laboratory settings, leading to decreased accuracy in viral DNA analysis. This could result in unreliable test results if the kit is used without the recall being addressed.

Who’s affected

Laboratory users who have the QIAamp DSP Virus Kit with the specific lot numbers listed in the recall are affected. Researchers and technicians working with viral DNA analysis are most at risk of inaccurate results.

How to tell if you have this one

Check the lot number on the QIAamp DSP Virus Kit packaging. Affected lots are 154025928, 154027751, 154029053, 154029743, and 154029744. The product is sold under Cat. No. 60704.

Brand
Qiagen
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Lot Number
Look for the lot number on the QIAamp DSP Virus Kit packaging to determine if it is affected.

✎ GovInfoNow

Questions people ask

Why is this kit being recalled?

The recall is due to potential decreased performance in analytic workflows, which could lead to inaccurate results.

Which lots are affected?

Affected lots are 154025928, 154027751, 154029053, 154029743, and 154029744.

Do I need to stop using the kit?

No, the recall does not require stopping use; it only affects specific lots that may cause decreased performance.

Take action

Contact Qiagen

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

✉️ Open in email

Subject: Recall Z-0274-2018 — Qiagen Qiagen

Hello,

I own a Qiagen that is covered by recall Z-0274-2018 from Qiagen.

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-0274-2018 (July 22, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0274-2018 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.

Qiagen, GmbH recalls QIAamp DSP Virus Kit Cat. No. 60704

Lower-risk recall