The Binding Site Group, Ltd.: Medical Device Recalls in 2021
Updated on March 25, 2026.
According to to data from the FDA, there were 3 medical device recalls made by The Binding Site Group, Ltd. in 2021. See the details of the recalls below.
You can see similar recalls for other firms.
Data Source: FDA.
- Optilite Freelite Mx Kappa Free Kit REF LK016.M.OPT.A
- Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the SPAPLUS) (x10) REF LK018.10S
- FREELITE Human Kappa Free Kit for use on the Roche cobas c Systems, Kappa Freie Leichtkette (Human) kit for Roche cobas c Systems, REF: LK016.CB, IVD CE, UDI: 05051700012096