Beckman Coulter recalls Uric Acid Reagent (URIC 2 X 300) for potential false test results due to acetaminophen interference. This may delay diagnosis and treatment. No remedy specified.
It has been determined that N-acetyl p benzoquinone imine (NAPQI), a metabolite of acetaminophen (paracetamol), may cause negative interference for assays if present in high quantities in serum due to acetaminophen overdoese. This could result in a delay in diagnosis and treatment.
Beckman Coulter is recalling Uric Acid Reagent (URIC 2 X 300) because it may cause false test results if acetaminophen is present in high amounts. This could delay diagnosis and treatment of conditions.
The reagent may interact with acetaminophen in the blood, causing false negative results in uric acid tests. This could lead to delayed diagnosis and treatment of conditions that require accurate uric acid measurements.
People using this reagent for in vitro diagnostic tests, especially those with acetaminophen in their serum. Those with medical conditions requiring frequent testing may be most at risk.
Check for the product name 'Uric Acid Reagent (URIC 2 X 300)' with reference number 442785. All lot numbers are affected. This product is for in vitro diagnostic use only and requires a prescription.
Verify the product name and reference number to confirm if it's affected.
The recall does not specify safety; it indicates potential for false test results due to acetaminophen interference.
The recall record does not provide a remedy, so no specific action is required beyond checking if you have the product.
The recall states it may delay diagnosis and treatment, but does not mention physical injury risks.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1424-2020 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1424-2020 from Beckman Coulter. 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.
