R&D Systems recalls Quantikine sTfR ELISA Kit (catalog DTFR1, lot P180851) due to incorrect control data card number. This may affect lab results accuracy for iron deficiency anemia testing.
The Human sTfR Quantikine IVD ELISA Kit, catalog # DTFR1, lot P180151 was packed with the incorrect control data card number 750228.4.
R&D Systems is recalling a specific sTfR ELISA kit used for iron deficiency anemia testing because it was packed with the wrong control data card number. This could lead to inaccurate lab results if the kit is used without proper calibration.
The kit was shipped with an incorrect control data card number (750228.4) instead of the correct one. This could cause inaccurate measurements of sTfR levels in blood samples, potentially leading to wrong diagnoses of iron deficiency anemia.
Lab technicians and healthcare providers who use the Quantikine sTfR ELISA Kit (catalog DTFR1, lot P180851) for iron deficiency anemia testing are most at risk. The recall affects only this specific batch.
Check for the catalog number DTFR1 and lot number P180851 on the kit packaging. The product is used for measuring sTfR in blood to help diagnose iron deficiency anemia.
Verify the catalog number DTFR1 and lot number P180851 on the kit's packaging.
The kit was packed with the incorrect control data card number 750228.4, which could cause inaccurate sTfR measurements for iron deficiency anemia testing.
Using this kit without the correct control data card may lead to inaccurate measurements of sTfR levels, potentially affecting iron deficiency anemia diagnoses.
The official recall does not provide a fix; users should check if they have the specific lot number and contact R&D Systems for further guidance.
We’ve drafted a message you can send R&D Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-0691-2019 — R&D Systems R&D Systems Hello, I own a R&D Systems that is covered by recall Z-0691-2019 from R&D Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
