Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Human Lambda Free SPAPlus Kit Product Code: LK018.S Freelite aids Recalled by The Binding Site Group, Ltd. Due to Calibration curve activity has increased over time in...
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 The Binding Site Group, Ltd. directly.
Affected Products
Human Lambda Free SPAPlus Kit Product Code: LK018.S Freelite aids in the detection and monitoring of Multiple Myeloma and related diseases.
Quantity: 1,002
Why Was This Recalled?
Calibration curve activity has increased over time in the kit lots listed.
Where Was This Sold?
This product was distributed to 11 states: AZ, CA, GA, HI, ID, MA, NY, OK, PA, TX, UT
About The Binding Site Group, Ltd.
The Binding Site Group, Ltd. has 28 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report