Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit Recalled by Diamedix Corporation Due to A gel-like substance was found in kit component,...
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 Diamedix Corporation directly.
Affected Products
Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and semi-quantitative detection of Mumps IgG antibodies as an aid in the diagnosis of Mumps infection.
Quantity: 697 kits
Why Was This Recalled?
A gel-like substance was found in kit component, sample diluent , that could potentially compromise product performance.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Diamedix Corporation
Diamedix Corporation has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report