The Binding Site Group, Ltd. recalls Human Lambda Free SPAPlus Kit Product Code: LK018.S Fr
See all recalls from The Binding Site Group, Ltd. →Recalled Product
Human Lambda Free SPAPlus Kit Product Code: LK018.S Freelite aids in the detection and monitoring of Multiple Myeloma and related diseases.
Hazard / Issue
Calibration curve activity has increased over time in the kit lots listed.
Issued by
FDA
Affected States: CA, TX, HI, GA, PA, UT, NY, OK, ID, MA, AZ
Lot/Code Info: Lot #323278, 327963
✅ What Should You Do?
- 1Contact your healthcare provider immediately to discuss this recall.
- 2Stop using the device if it is safe to do so, and contact your provider.
- 3Follow the manufacturer's remedy instructions provided in the recall notice.
- 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Human Lambda Free SPAPlus →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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