Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
CK MB Calibrator Recalled by Randox Laboratories Ltd. Due to Randox have realigned CK-MB Calibrator, CK2393, lot number...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Randox Laboratories Ltd. directly.
Affected Products
CK MB Calibrator, Catalogue Number CK2393
Quantity: 1,392
Why Was This Recalled?
Randox have realigned CK-MB Calibrator, CK2393, lot number 4410CK. Calibrating with the new value will cause a positive shift of approximately 6% with both Quality Controls and Patient Samples.
Where Was This Sold?
This product was distributed to 1 state: WV
About Randox Laboratories Ltd.
Randox Laboratories Ltd. has 72 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report