Randox recalls Liquid Cardiac Control models CQ5051-53 for possible NTproBNP measurement errors on Siemens Dimension EXL LOCI systems. Affected units may show lower results than expected.
Customers may observe a decrease in recovered concentration with regards to NTproBNP in the Liquid Cardiac Control lots identified, on the Siemens Dimension EXL LOCI.
Randox is recalling Liquid Cardiac Control test kits with model numbers CQ5051, CQ5052, and CQ5053. These kits might give lower results for NTproBNP measurements on specific lab equipment, which could affect heart health assessments.
The Liquid Cardiac Control kits may produce lower NTproBNP readings than expected when used with Siemens Dimension EXL LOCI systems. This could lead to incorrect heart health assessments if the test results are not properly interpreted.
Healthcare labs using Siemens Dimension EXL LOCI systems with the specified model numbers and lots are likely affected. Patients relying on these tests for heart health monitoring may be at risk of inaccurate results.
Check for model numbers CQ5051, CQ5052, or CQ5053 on the kit. Affected lots are 4243CK, 4244CK, or 4245CK. These kits were sold with Siemens Dimension EXL LOCI systems.
Look for model numbers CQ5051, CQ5052, or CQ5053 on the Liquid Cardiac Control kit.
Confirm the lot number is 4243CK, 4244CK, or 4245CK for affected units.
The recall is for potential NTproBNP measurement errors in specific Liquid Cardiac Control kits used with Siemens Dimension EXL LOCI systems.
No, the recall does not require immediate stop use. Affected kits may still be used but could produce inaccurate results.
Check for model numbers CQ5051, CQ5052, or CQ5053 and lot numbers 4243CK, 4244CK, or 4245CK.
We’ve drafted a message you can send Randox to request your refund or repair — edit it as you like.
Subject: Recall Z-1785-2019 — Randox Randox Hello, I own a Randox that is covered by recall Z-1785-2019 from Randox. 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.
