Chromsystems recalls MassCheck Amino Acid, Acylcarnitines Dried Blood Spot Control Level II batch 2821 due to low glycine concentration. Affected units may not provide accurate blood testing results.
Too low concentration of glycine was detected in the dried blood controls of the batch 2821 of the products.
Chromsystems is recalling a specific batch of dried blood spot controls because they contain too little glycine. This could lead to inaccurate blood test results if used in medical testing. The affected batch number is 2821.
The dried blood controls have too low a concentration of glycine, which is a critical component for accurate blood testing. This could cause inaccurate results if the controls are used in medical testing procedures.
Users of the MassCheck Amino Acid, Acylc:arnitines Dried Blood Spot Control Level II product with batch number 2821 are affected. Healthcare providers and labs using this specific batch for blood testing may be at risk.
Check the lot number on the product label. The affected batch is 2821. The product model is 0193.
Look for the lot number 2821 and model number 0193 on the product label.
The affected batch number is 2821.
Check the lot number on the product label; the affected batch is 2821 with model number 0193.
The recall record does not specify a remedy, so no action is required beyond checking the product label.
We’ve drafted a message you can send Chromsystems to request your refund or repair — edit it as you like.
Subject: Recall Z-1337-2022 — Chromsystems Chromsystems Hello, I own a Chromsystems that is covered by recall Z-1337-2022 from Chromsystems. 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.
