Nature-Throid recalled over manufacturing violations
- Recall date
- August 25, 2020
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- RLC Labs Inc. recalls Nature-Throid, Thyroid USP [liothyronine (T3) 6.75 mcg and levothyroxine (T4) 28.5 mcg], 3/4 Grain (48.75 mg) Tablets,…
- Recall number
- D-1597-2020
- FDA classification
- Class II
- Brand / firm
- RLC Labs Inc.
- Sold / distributed
- Nationwide in the United States
Why it was recalled
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Nature-Throid, Thyroid USP [liothyronine (T3) 6.75 mcg and levothyroxine (T4) 28.5 mcg], 3/4 Grain (48.75 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3302-4; b) 60-count bottles, NDC 64727-3302-5; c) 90-count bottles, NDC 64727-3302-6; d) 100-count bottles, NDC 64727-3302-1; and e) 1,000-count bottles, NDC 64727-3302-2; Rx Only, Manufactured by: RLC Labs Phoenix, AZ 85034.
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