Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Liquid Cardiac Control CQ5053 Recalled by Randox Laboratories, Limited Due to Randox has confirmed that Troponin T and Troponin...

Date: August 8, 2017
Company: Randox Laboratories, Limited
Status: Terminated
Source: FDA (Device)

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, Limited directly.

Affected Products

Liquid Cardiac Control CQ5053

Quantity: 450 kits

Why Was This Recalled?

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.

Where Was This Sold?

Nationally

About Randox Laboratories, Limited

Randox Laboratories, Limited has 13 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report