GMP Laboratories of Lithium Orotate, Weyland Brain Nutrition recall — FDA H-0448-2025
Downstream recall of a dietary supplement ingredient that was manufactured out of specification.
Overview of recall records associated with GMP Laboratories of America Inc, including dates, categories and classifications where available.
Classification mix: Class III: 2.
Downstream recall of a dietary supplement ingredient that was manufactured out of specification.
Downstream recall of a dietary supplement ingredient that was manufactured out of specifications.
This page summarizes recall records in which the official source identifies GMP Laboratories of America Inc 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.