Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1422-2022 — Soluble Transferrin Receptors (STFR), Catalog Number TF10159 (Research Use Only). IVD

U.S. FDA — Device Enforcement · Ireland · 2022-06-09 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1422-2022
Date of alert
2022-06-09
Country / jurisdiction
Ireland
Risk level
Class III
Risk type
recall
Brand
Randox Laboratories Ltd.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
05055273215564
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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