Cytocell recalls Aquarius CSF1R/RPS14 Probe Red reagent (model LPH540-A) with lot numbers 056996, 061156, 062616, 062808 due to a labeling error in the chromomap.
There is an error in the chromomap included in the labeling for the product.
Cytocell is recalling a specific reagent used in laboratory testing because the labeling contains an error in the chromomap. This error could lead to incorrect test results if the reagent is used without proper understanding of the labeling.
The labeling error in the chromomap could cause laboratory users to misinterpret the product's specifications, potentially leading to inaccurate test results. This is a technical error that does not pose a physical safety risk but affects the accuracy of the reagent's use.
Laboratory users who purchased the Aquarius CSF1R/RPS14 Probe Red reagent (model LPH540-A) with lot numbers 056996, 061156, 062616, or 062808 are affected. Researchers and technicians working with this reagent are most at risk of incorrect test results.
Check the lot number on the reagent's packaging. The affected model is LPH540-A with lot numbers 056996, 061156, 062616, or 062808. This reagent is used in laboratory settings for specific analyte testing.
Look for the lot numbers 056996, 061156, 062616, or 062808 on the reagent packaging.
The recall is due to an error in the chromomap included in the labeling, which could lead to incorrect test results if the reagent is used without proper understanding of the labeling.
The official recall notice does not specify a remedy, so you should check the lot number and contact Cytocell Ltd. for further instructions.
No, the recall is for a labeling error that affects test accuracy, not a physical safety hazard.
We’ve drafted a message you can send Cytoc:ell to request your refund or repair — edit it as you like.
Subject: Recall Z-1202-2019 — Cytoc:ell Cytoc:ell Hello, I own a Cytoc:ell that is covered by recall Z-1202-2019 from Cytoc:ell. 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.
