Advance Dx recalls 25-count blood collection cards and 500-pack foil bags due to high glucose test results. Consumers should check product details and contact the company for remedy.
Due to high glucose test results when using the blood collection cards.
Advance Dx is recalling blood collection cards and foil bags that may cause high glucose test results. This could lead to inaccurate blood sugar readings, which might affect health decisions.
The blood collection cards may produce high glucose test results when used with certain blood samples. This could lead to inaccurate blood sugar readings, potentially causing health decisions based on incorrect information.
People who use these blood collection cards for glucose testing may be affected. Those with diabetes or health conditions requiring regular glucose monitoring are at higher risk.
Check for product catalog number CMT01 or lot number PPD02102 on the packaging. The product was sold with the reference code REF CMT01.
Look for product catalog number CMT01 or lot number PPD02102 on the packaging.
The blood collection cards may cause high glucose test results, leading to inaccurate blood sugar readings.
Check for product catalog number CMT01 or lot number PPD02102 on the packaging.
The official recall notice does not specify a remedy or action for affected consumers.
We’ve drafted a message you can send Advance Dx to request your refund or repair — edit it as you like.
Subject: Recall Z-2237-2021 — Advance Dx Advance Dx Hello, I own a Advance Dx that is covered by recall Z-2237-2021 from Advance Dx. 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.
