RecallWatchUSA

Home / Recalls / Medical Devices

The Binding Site Group, Ltd. recalls C-Reactive Protein Kit for use on the SPAplus, REF NK044.S.A, Rx only, UDI (01)05051700018456,

Recalled April 8, 2020 · FDA recall Z-1619-2020 · The Binding Site Group

Hazard
A reagent in C reactive protein kits is not performing to specification and samples with known concentrations less-than-or-equal to 10 mg/L may be affected · FDA Class II
Units
1 kit
Sold at
U.S.: FL

Description

A reagent in C reactive protein kits is not performing to specification and samples with known concentrations less-than-or-equal to 10 mg/L may be affected

Product
C-Reactive Protein Kit for use on the SPAplus, REF NK044.S.A, Rx only, UDI (01)05051700018456,
Manufacturer(s)
The Binding Site Group, Ltd.
Made in
United Kingdom

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

The Binding Site Group, Ltd. recalls C-Reactive Protein Kit for use on the SPAplus, REF NK044.S.A, Rx only, UDI (01)05051700018456, | RecallWatchUSA