Randox recalls Liquid Cardiac Control CQ5053 lot 4069CK due to shelf-life issues. The control may fall outside specified ranges, affecting accuracy.
Randox has confirmed that Troponin T and Troponin I in Liquid Cardiac quality control CQ5053 lot 4069CK does not meet the shelf-life claim in the product labelling. As the control may now fall outside the provided control ranges the product is to be recalled from the field.
Randox is recalling a specific batch of Liquid Cardiac Control CQ5053 (lot 4069CK) because it may no longer meet the shelf-life claim on the label. This could cause the test results to be outside the expected control ranges, potentially leading to inaccurate cardiac tests.
The product may no longer meet the shelf-life claim on its label. This means the control could fall outside the specified test ranges, leading to inaccurate cardiac test results if used.
Healthcare professionals using this specific batch of Liquid Cardiac Control CQ5053 for cardiac testing are affected. Those who have this lot number are most at risk of inaccurate test results.
Check for the product name 'Liquid Cardiac Control CQ5053' and lot number 4069CK on the label. This specific batch is being recalled.
Look for the lot number 4069CK on the Liquid Cardiac Control CQ5053 product label.
No, this is a low-risk issue. The product may not meet shelf-life claims, but it does not pose a direct safety hazard.
Check for the product name 'Liquid Cardiac Control CQ5053' and lot number 4069CK on the label.
The recall record does not specify a remedy, so contact Randox Laboratories for guidance.
We’ve drafted a message you can send Randox to request your refund or repair — edit it as you like.
Subject: Recall Z-0937-2018 — Randox Randox Hello, I own a Randox that is covered by recall Z-0937-2018 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.
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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.
