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Recall Observatory FDA recall evidence

Device product

Liquid Cardiac Control - Level 3, cat. no. CQ5053 Product Usage: This product is intended for in vitro diagnostic use, in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems.

Z-2575-2018

June 08, 2018

Class II

Product summary

Firm
Randox Laboratories Ltd.
Event
Event 80475
Status
Terminated
Classification
Class II
Quantity
1 kit (US), 602 kits (OUS)
Official record key
device-enforcement:Z-2575-2018

Official wording

Reason: The device is not suitable for the control of the Troponin T assay due to unacceptable variation between vials. The deviation in precision observed is up to 28%. IQC that is reported as out of range could lead to a delay in reporting Troponin T results. If the failure occurs the operator may observe the quality control result for Troponin T falling outside range and/or increased imprecision for Quality Control monitoring.

Code information: Lot 4245CK.

Distribution pattern: Worldwide Distribution - US in the state of WV. Foreign distribution to Australia, Chile, China, Germany, Hungary, Ireland, Italy, Moldova, Netherlands, Peru, Poland, Saudi Arabia, Slovakia, Spain, Sultanate of Oman, UAE, UK, and Vietnam

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The device is not suitable for the control of the Troponin T assay due to unacceptable variation between vials. The deviation in precision observed is up to 28%. IQC that is reported as out of range could lead to a delay in reporting Troponin T results. If the failure occurs the operator may observe the quality control result for Troponin T falling outside range and/or increased imprecision for Quality Control monitoring.