Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EliA RF IgM Well Recalled by Phadia Ab Due to Potential for reporting low assay results
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Phadia Ab directly.
Affected Products
EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro quantitative measurement of IgM class rheumatoid factor antibodies in human serum and plasma (Li-heparin and EDTA) to aid in the diagnosis of rheumatoid arthritis in conjunction with other laboratory and clinical findings. EliA RF IgM uses the EliA IgM method on the instrument Phadia 100, Phadia 250, Phadia 2500 and Phadia 5000.
Quantity: 30 kits
Why Was This Recalled?
Potential for reporting low assay results
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Phadia Ab
Phadia Ab has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report