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The Binding Site Group, Ltd. recalls Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S, LK018.10S Freelite aids the detection and m
Recalled January 25, 2017 · FDA recall Z-1053-2017 · The Binding Site Group
Hazard
A change in the calibration curve causing an increase in false prozone flags. · FDA Class II
Units
3,088
Sold at
Worldwide Distribution - U.S. (nationwide) and Internationally to the following; Canada, Australia.
Description
A change in the calibration curve causing an increase in false prozone flags.
Product
Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S, LK018.10S Freelite aids the detection and monitoring of Multiple Myeloma and related diseases
Manufacturer(s)
The Binding Site Group, Ltd.
Made in
United Kingdom
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →