Beckman Coulter recalls Access Vitamin B12 Reagent lot 439850 due to potential erroneous Vitamin B12 results, which could lead to delayed or improper diagnosis. Affected units may need replacement.
Beckman Coulter has received complaints of erroneous Vitamin B12 results when using Access Vitamin B12 Reagent lot 439850. The affected reagent lot may cause erroneously low or high Vitamin B12 results, leading to a delayed or improper diagnosis and/or repeat testing.
Beckman Coulter is recalling Access Vitamin B12 Reagent lot 439850 because it may cause inaccurate Vitamin B12 test results. This could lead to delayed or improper diagnosis and repeat testing. The recall affects users who have this specific lot number.
The reagent lot 439850 may produce erroneous Vitamin B12 results, causing either falsely low or high readings. This could lead to delayed or improper diagnosis and repeat testing, potentially affecting medical treatment decisions.
Users of the Access Vitamin B12 Reagent lot 439850 are affected. Those who rely on this reagent for medical testing may be at risk of inaccurate results.
Check the lot number on the reagent bottle. The affected lot is 439850. This reagent is sold under catalog number 33000.
Look for the lot number 439850 on the reagent bottle to confirm if it is affected.
Beckman Coulter has received complaints of erroneous Vitamin B12 results when using Access Vitamin B12 Reagent lot 439850.
The affected reagent may cause erroneously low or high Vitamin B12 results, leading to delayed or improper diagnosis and repeat testing.
Check the lot number on the reagent bottle; the affected lot is 439850.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-2115-2025 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-2115-2025 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.
