Carolina Liquid Chemistries recalls Etha Rgt Kit (IVD, REF ST321) due to absorbance rate not meeting quality standards. Defective lots may not function by end of shelf life.
Supplier testing showed that the absorbance rate of the Ethyl Alcohol Assay did not meet internal quality control specifications. The defective lots will not function toward the end of shelf life.
Carolina Liquid Chemist: Etha Rgt Kit (IVD, REF ST321) is recalled because supplier testing found the absorbance rate didn't meet quality control standards. This means the defective kits won't work properly by the end of their shelf life.
The absorbance rate of the Ethyl Alcohol Assay in the kit did not meet internal quality control specifications. This means the defective lots will not function properly toward the end of their shelf life, potentially leading to inaccurate test results.
Users of the Etha Rgt Kit (IVD, REF ST321) with lot number 11687 are affected. Laboratory or clinical staff using this kit for alcohol assays are most at risk.
Check for the product name 'Etha Rgt Kit' (IVD, REF ST321) and lot number 11687 on the packaging. This kit is sold by Carolina Liquid Chemistries.
Verify the product name and lot number on the packaging to confirm if it's the recalled Etha Rgt Kit (IVD, REF ST321, Lot 11687).
Supplier testing showed the absorbance rate of the Ethyl Alcohol Assay did not meet internal quality control specifications.
The official recall notice does not specify a remedy or action steps beyond checking product details.
The defective lots will not function properly toward the end of their shelf life.
We’ve drafted a message you can send Carolina Liquid Chemistries to request your refund or repair — edit it as you like.
Subject: Recall Z-1253-2019 — Carolina Liquid Chemistries Carolina Liquid Chemistries Hello, I own a Carolina Liquid Chemistries that is covered by recall Z-1253-2019 from Carolina Liquid Chemistries. 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.
