Randox recalls specific Lipase Colorimetric R2 Substrate batches due to imprecision in patient sample testing. Affected units may yield inaccurate lipase test results.
Randox have confirmed imprecision of quality control and patient samples when using specific Randox Lipase R2 Substrate batches.
Rando: Randox has recalled specific batches of Lipase Colorimetric R2 Substrate due to imprecision in patient sample testing. This could lead to inaccurate lipase test results for blood tests.
The recalled batches have imprecision in quality control, meaning patient samples may not be tested accurately. This could lead to incorrect lipase test results for blood tests.
People who use Randox Lipase Assay R2 Substrate for blood tests may be affected. Those with specific batch numbers are most at risk.
Check for batch numbers 1049LI or 1051LI on the Randox Lipase R2 Substrate packaging. The product is sold under catalogue numbers LI015/000/UL and LI015/003/UL.
Look for batch numbers 1049LI or 1051LI on the Randox Lipase R2 Substrate packaging.
The recalled batches have imprecision in quality control, meaning patient samples may not be tested accurately.
Batch numbers 1049LI and 1051LI are affected.
Check for batch numbers 1049LI or 1051LI on the Randox Lipase R2 Substrate packaging. The product is sold under catalogue numbers LI015/000/UL and LI015/003/UL.
We’ve drafted a message you can send Randox to request your refund or repair — edit it as you like.
Subject: Recall Z-2753-2020 — Randox Randox Hello, I own a Randox that is covered by recall Z-2753-2020 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.
