Herbal Doctor Remedies Cardia Forte, 500 mg Capsules, 90-count bottles, Herbal Doctor recall — FDA D-1592-2019
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Overview of recall records associated with Herbal Doctor Remedies, including dates, categories and classifications where available.
Classification mix: Class II: 76.
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
This page summarizes recall records in which the official source identifies Herbal Doctor Remedies 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.