FDA recall record

Randox Laboratories Soluble Transferrin Receptors Calibrator Series (STFR CAL), Catalog recall — FDA Z-1423-2022

A customer reported a problem with the reagent and calibrator. Randox Laboratories carried out an investigation and confirmed the issue. The complaint is…

Class IIIclassification
Z-1423-2022official record ID
Jul 27, 2022report date

Recall record at a glance

Official recordZ-1423-2022
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmRandox Laboratories Ltd.
Report dateJul 27, 2022
Recall initiation dateJun 9, 2022
Quantity12 kits (US)
LocationCrumlin (North), N/A, Ireland

Official product description

Soluble Transferrin Receptors Calibrator Series (STFR CAL), Catalog Number TF10161. IVD

Why the product was recalled

A customer reported a problem with the reagent and calibrator. Randox Laboratories carried out an investigation and confirmed the issue. The complaint is pertaining to atypical calibration curves that can results in non-numerical results. This affects Siemens Atellica CH analysers only. Customer have reported an atypical calibration curve that results in the values around the low QC range to produce a non-numerical result. It appears to be related to the bottle values of the calibrator producing a curve shape that is too linear for the logitlog calculation to calculate. This issue can only be identified in the Atellica graphical view of the calibration. In most of the cases when this has occurred, it is picked up by the QC generating a Math Error, however, there are reports of QC shifts after calibration without the Math Error flagged that may be related to this issue. Results reported with STFR Level 1, with a concentration less than 1.7mg/L, using TF10159 and TF10161 can be underestimated by up to 30%. This issue has been reported with reagent lots 575475 and 562691, calibrator lots 537725 and 562696. No other complaints received.

Distribution information

US Nationwide distribution in the state of IL.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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