Medical DeviceDec 3, 2014
Biomerica Calcitonin ELISA Kit, Code No. 7024, 7024BU recall — FDA Z-0467-2015
A potential issue with false high values.
Class IIFDA: TerminatedBiomerica
Overview of recall records associated with Biomerica, including dates, categories and classifications where available.
Classification mix: Class II: 1.
A potential issue with false high values.
This page summarizes recall records in which the official source identifies Biomerica as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.