Randox recalls Liquid Clinical Chemistry Control (LAE4217) due to incorrect lipase value in specific lot. This may affect lab test accuracy. No action needed for most users.
A transcription error has occurred for the Randox Lipase colorimetric value in Liquid Clinical Chemistry Control lot 1021 UE. The target and range are listed as 50 U/L (40 - 60) and should be 72U/L (58 - 86).
Randox is recalling a specific lot of their Liquid Clinical Chemistry Control (LAE4217) because the lipase value listed on the product is incorrect. This could lead to inaccurate lab test results if the product is used. The recall only affects a specific lot number.
The product lists a lipase value of 50 U/L (40-60) when it should be 72 U/L (58-86). This transcription error could cause lab tests to give inaccurate results if the product is used in clinical testing.
Lab users who purchased the specific lot (1021UE) of Randox Liquid Clinical Chemistry Control (LAE4217) are affected. Most users are not at risk as this is a specific lot with no widespread distribution.
Check for the lot number 1021UE on the product label. The product is labeled as Liquid Clinical Chemistry Control, Catalogue Number LAE4217, with an expiration date of June 28, 2020.
Look for the lot number 1021UE on the product label to confirm if it is affected.
No, this is a transcription error that could affect lab test accuracy but does not pose a physical danger to users.
No action is needed for most users. Only the specific lot 1021UE is affected, and the product is not dangerous to handle.
Check the product label for the lot number 1021UE. The product is labeled as Liquid Clinical Chemistry Control, Catalogue Number LAE4217, with an expiration date of June 28, 2020.
We’ve drafted a message you can send Randox to request your refund or repair — edit it as you like.
Subject: Recall Z-1100-2020 — Randox Randox Hello, I own a Randox that is covered by recall Z-1100-2020 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.
