Cardia Forte recalled over manufacturing violations
- Recall date
- July 12, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Herbal Doctor Remedies recalls Cardia Forte, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
- Recall number
- D-1592-2019
- FDA classification
- Class II
- Brand / firm
- Herbal Doctor Remedies
- Sold / distributed
- Nationwide within the United States and Brazil and on the internet
Why it was recalled
CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Cardia Forte, 500 mg Capsules, 90-count bottles, Herbal Doctor Remedies Alhambra, CA 91801-7081 USA, 1(800) 600-0808
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