Z-1423-2022 Class III Terminated

Recalled by Randox Laboratories Ltd. — Crumlin (North), N/A

FDA device recall Z-1423-2022 was initiated by Randox Laboratories Ltd. on Jun 9, 2022 and is designated Class III. Reason for recall: 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… The recall status is terminated (terminated Feb 8, 2024). Affected quantity: 12 kits (US).

Recall Details

Product Type
Devices
Report Date
Jul 27, 2022
Initiation Date
Jun 9, 2022
Termination Date
Feb 8, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
12 kits (US)

Product Description

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

Reason for Recall

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 Pattern

US Nationwide distribution in the state of IL.

Code Information

UDI-DI (GTIN): 05055273215557 All lots within expiry

Source

Dataset
openFDA device recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for Z-1423-2022
openFDA file date
Oct 23, 2026
Loaded by RegDataLab
Oct 25, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.