Reported Jan 25, 2017 · Terminated
Freelite Human Lambda Free Kit for use on SPAPLUS Product Code: LK018.S, LK018.10S Freelite aids the detection and…
The Binding Site Group, Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: The Binding Site Group, Ltd. · 8 Calthorpe Road · Birmingham · N/A
Is this the product you have?
- Freelite Human Lambda Free
- Kit for use on SPAPLUS Product CodeLK018.S, LK018.10S Freelite aids the detection and monitoring of Multiple Myeloma and related diseases
- Lot codes and dates
Lot #400012400257
- Amount recalled
- 3,088
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
- Nationwide
Why it was recalled
A change in the calibration curve causing an increase in false prozone flags.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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