Soluble Transferrin Receptors recall
Soluble Transferrin Receptors (STFR), Catalog Number TF10159 (Research Use Only). IVD
Why was Soluble Transferrin Receptors 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI-DI (GTIN): 05055273215564 All lots within expiry
- Product
- Soluble Transferrin Receptors (STFR), Catalog Number TF10159 (Research Use Only). IVD
- Recalling firm
- Randox Laboratories Ltd.
- Quantity
- 12 kits (US)
- Distribution
- US Nationwide distribution in the state of IL.
- Recall date
- July 27, 2022
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)