Randox recalls specific lipase reagent batches due to imprecision in patient sample testing. Affected products include LI3837, LI7979, LI8050, LI8361 with certain lot numbers. Users should stop using these reagents to prevent inaccurate test results.
Randox have confirmed imprecision of quality control and patient samples when using specific Randox Lipase reagent batches.
Randox is recalling specific batches of lipase reagents used in blood tests because they can produce inaccurate results when testing patient samples. This could lead to incorrect medical diagnoses if the reagents are used without replacement.
The reagents have imprecision in quality control, meaning they can give inaccurate results when testing patient samples. This could lead to incorrect medical diagnoses if the reagents are used without replacement.
Healthcare professionals using Randox lipase reagents for blood tests are affected. Patients receiving tests with these specific reagent batches may be at risk of incorrect results.
Check the product catalog numbers: LI3837, LI7979, LI8050, or LI8361. Look for lot numbers 507360, 497086, 497053, 497038, or 502135 on the packaging.
Immediately stop using the affected reagent batches to prevent inaccurate test results.
Affected batches include LI3837, LI7979, LI8050, LI8361 with lot numbers 507360, 497086, 497053, 497038, and 502135.
Randox has confirmed imprecision in quality control and patient samples when using specific reagent batches.
Yes, if you have the affected batches, you should stop using them and replace with a different reagent.
We’ve drafted a message you can send Randox to request your refund or repair — edit it as you like.
Subject: Recall Z-2751-2020 — Randox Randox Hello, I own a Randox that is covered by recall Z-2751-2020 from Randox. 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.
