Beckman Coulter recalls 4x25 mL Bicarbonate reagent (OSR6137) due to potential calibration failures. Affected lots: UDI-GI: 15099590020187. No remedy stated in official notice.
There is a potential for a decrease in calibration ODs for Bicarbonate reagent which could result in calibration failures and/or quality control failures.
Beckman Coulter is recalling 4x25 mL Bicarbonate reagent (OSR6137) because it may cause calibration failures in lab equipment. This could lead to inaccurate test results or quality control issues in laboratory settings.
The reagent may cause calibration failures in laboratory equipment, leading to inaccurate test results or quality control issues. This happens because the reagent's calibration could decrease, affecting the accuracy of measurements.
Laboratory users who own or use the recalled Bicarbonate reagent (UDI-GI: 15099590020187) are affected. Researchers and lab technicians using this specific reagent are most at risk of inaccurate test results.
Check for the product name 'Beckman Coulter Bicarbonate', reference number OSR6137, and lot number UDI-GI: 15099590020187. The product is sold in 4x25 mL vials.
Identify the product name, reference number OSR6137, and lot number UDI-GI: 15099590020187 to confirm if it's affected.
The official recall notice does not state any remedy or fix for this product.
The recall notice does not specify any action steps beyond identifying the affected product.
Check for the product name 'Beckman Coulter Bicarbonate', reference number OSR6137, and lot number UDI-GI: 15099590020187.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1606-2023 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1606-2023 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.
