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Recall Observatory FDA recall evidence

Device product

Randox Rx Series Mg - Product Usage: For the quantitative in vitro determination of Magnesium in serum, plasma and urine Catalogue Number: MG8326

Z-0547-2021

November 13, 2020

Class II

Product summary

Firm
Randox Laboratories Ltd.
Event
Event 86827
Status
Terminated
Classification
Class II
Quantity
4 kits
Official record key
device-enforcement:Z-0547-2021

Official wording

Reason: Failing to meet the linearity performance claims quoted on the kit inserts-The linearity is reduced by approximately -30% for Serum/ Plasma and -50% for Urine

Code information: Lot Number: 539770 Exp. Date : 28 March 2022 UDI: 05055273209303

Distribution pattern: US Nationwide distribution in the states of GA, NJ.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Failing to meet the linearity performance claims quoted on the kit inserts-The linearity is reduced by approximately -30% for Serum/ Plasma and -50% for Urine