Home / Recalls / The Binding Site Group, Ltd. / Z-1053-2017

Z-1053-2017 Class II Terminated

Recalled by The Binding Site Group, Ltd. — Birmingham

Recall Details

Product Type
Devices
Report Date
January 25, 2017
Initiation Date
October 28, 2016
Termination Date
July 27, 2017
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
3,088

Product Description

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

Reason for Recall

A change in the calibration curve causing an increase in false prozone flags.

Distribution Pattern

Worldwide Distribution - U.S. (nationwide) and Internationally to the following; Canada, Australia.

Code Information

Lot #400012, 400257

Other recalls by The Binding Site Group, Ltd.

  • Z-0274-2022 Class II — Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Hu (October 15, 2021)
  • Z-2030-2021 Class II — FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems, Kappa Freie (May 20, 2021)
  • Z-0943-2021 Class II — Optilite Freelite Mx Kappa Free Kit REF LK016.M.OPT.A (November 18, 2020)
  • Z-2071-2020 Class II — The Optilite Clinical Chemistry Analyzer. IVD. Model Number: IE700. UDI-05051700 (April 9, 2020)
  • Z-1500-2020 Class II — Rheumatoid Factor (RF) Kit for use on SPAPLUS, for in-vitro diagnostic use, Prod (November 6, 2019)
  • Z-2110-2020 Class II — Optilite Optilite Rheumatoid Factor Kit, Ref: LK151.OPT.A, IVD, Rx Only, UDI: (October 7, 2019)
  • Z-1327-2020 Class II — OPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 05051700017565 (July 29, 2019)
  • Z-1619-2020 Class II — C-Reactive Protein Kit for use on the SPAplus, REF NK044.S.A, Rx only, UDI (01)0 (April 25, 2019)
  • Z-0671-2020 Class II — Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive Protein (February 19, 2019)
  • Z-0604-2019 Class II — Binding Site Human IgM Kit (for SPAPLUS), REF: NK012.S The device consists of (November 6, 2018)