Beckman Coulter recalls 4x50 mL Bicarbonate reagent (Lot UDI-GI: 15099590010348) due to potential calibration failures. Consumers should check product details and contact the manufacturer for guidance.
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 4x50 mL Bicarbonate reagent (Lot UDI-GI: 15099590010348) because it may cause calibration failures in laboratory testing. This could lead to inaccurate results if used in sensitive equipment.
The reagent may cause calibration failures in laboratory equipment, leading to inaccurate test results. This happens because the reagent's calibration could drift over time, affecting the precision of measurements.
Laboratory users who own or use the recalled Bicarbonate reagent (Lot UDI-GI: 15099590010348) are affected. Those using the reagent for critical testing may be at higher risk of inaccurate results.
Check for the product name 'Beckman Coulter Bicarbonate' and the lot number UDI-GI: 15099590010348 on the packaging. The product was sold with the reference code OSR6237.
Identify the lot number UDI-GI: 15099590010348 on the packaging to confirm if the product is recalled.
The recall is for potential calibration failures, not immediate safety risks. The product is safe to use but may cause inaccurate test results if calibration fails.
Check for the lot number UDI-GI: 15099590010348 on the packaging of Beckman Coulter Bicarbonate (4x50 mL, reference OSR6237).
The recall does not specify a remedy, so contact Beckman Coulter directly for guidance on next steps.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1607-2023 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1607-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
