Accriva Diagnostics recalls directCHECK ACT-LR whole blood quality control level 2 (DCGLR-2) due to incorrect performance range labeling on the control kit.
Assayed Whole blood control contains labeling with incorrect performance range.
Accriva Diagnostics is recalling directCHECK ACT-LR whole blood quality control level 2 (DCGLR-2) because the labeling shows an incorrect performance range. This could lead to inaccurate blood test results if used in a lab setting.
The control kit has labeling that shows an incorrect performance range for blood tests. This could cause inaccurate test results if the lab uses the kit without noticing the error. However, the product itself is still safe to use.
Lab technicians and medical facilities that use this specific blood quality control kit for testing. The risk is low as the issue is with labeling, not the product's function.
Check for the model DCGLR-2 with lot number A6DLA001 or unique device identifier 10711234170373. This specific blood quality control kit is used in labs for whole blood testing.
Verify the performance range on the label matches the correct specifications for accurate blood testing.
Yes, the product is safe to use but the labeling shows an incorrect performance range, which could lead to inaccurate test results.
Look for the model DCGLR-2 with lot number A6DLA001 or unique device identifier 10711234170373.
No, the product is safe to use but you should check the labeling for the correct performance range to ensure accurate test results.
We’ve drafted a message you can send Accr: a short, human brand name for headings (e.g. to request your refund or repair — edit it as you like.
Subject: Recall Z-2460-2026 — Accr: a short, human brand name for headings (e.g. Accr: a short, human brand name for headings (e. Hello, I own a Accr: a short, human brand name for headings (e.g. that is covered by recall Z-2460-2026 from Accr: a short, human brand name for headings (e.g.. 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.
