Beckman Coulter recalls 4x173mL Bicarbonate reagent (OS6637) due to potential calibration failures. Affected lots: UDI-GI: 15099590060206. No remedy specified in recall 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 4x173 mL Bicarbonate reagent (OS6637) because it may cause calibration failures in laboratory equipment. This could lead to inaccurate test results and quality control issues if used improperly.
The reagent may cause calibration failures in laboratory equipment, leading to inaccurate test results and quality control issues. This happens because the reagent's calibration ODs could decrease, affecting the precision of measurements.
Laboratory users who purchased the Beckman Coulter Bicarbonate reagent (OS6637) with UDI-GI code 15099590060206 are affected. Researchers and lab technicians using this reagent for calibration purposes are most at risk of inaccurate test results.
Check for the product name 'Beckman Coulter Bicarbonate', reference code OS6637, and quantity 4x173 mL. The unique identifier UDI-GI: 15099590060206 identifies the affected lot.
Verify the product name, reference code OS6637, and quantity 4x173 mL to confirm if it matches the recalled item.
The recall notice does not specify any remedy or corrective action.
The recall notice does not provide specific instructions for affected users.
Check for the product name 'Beckman Coulter Bicarbonate', reference code OS6637, and quantity 4x173 mL with UDI-GI: 15099590060206.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1608-2023 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1608-2023 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.
