QIAGEN recalls EZ1 DSP Virus Kit (48) for potential incorrect test results from underfilled reagent wells. Affected units have specific UDI and lot numbers.
Underfilled reagent well that could lead to incorrect results
QIAGEN is recalling its EZ1 DSP Virus Kit (48) because underfilled reagent wells might cause incorrect test results. This affects laboratory users who rely on the kit for in vitro diagnostics.
The kit's reagent wells may be underfilled, leading to inaccurate test results. This could affect the reliability of diagnostic tests if the kit is used without proper filling.
Laboratory users who purchased the EZ1 DSP Virus Kit (48) with UDI 04053228000099 and lot number 160020069 are most at risk. The recall targets specific units sold for in vitro diagnostic testing.
Check for the UDI code 04053228000099 and lot number 160020069 on the kit's packaging. The product was sold for in vitro diagnostic use with an expiration date of November 1, 2019.
Verify the UDI code 04053228000099 and lot number 160020069 on the kit's packaging.
The recall is due to underfilled reagent wells that could lead to incorrect test results.
Check the UDI code and lot number on the packaging to see if it matches the recalled units. If it does, contact QIAGEN for further instructions.
The recall addresses potential incorrect test results, not physical injury risks. The hazard level is low risk.
We’ve drafted a message you can send QIAGEN to request your refund or repair — edit it as you like.
Subject: Recall Z-2596-2018 — QIAGEN QIAGEN Hello, I own a QIAGEN that is covered by recall Z-2596-2018 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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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.
