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) 9 mcg and levothyroxine (T4) 38 mcg], 1 Grain (65 mg) Tablets, packaged i…
- Recall number
- D-1596-2020
- 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) 9 mcg and levothyroxine (T4) 38 mcg], 1 Grain (65 mg) Tablets, packaged in a) 30-count bottles, NDC 64727-3300-4; b) 60-count bottles, NDC 64727-3300-5; c) 90-count bottles, NDC 64727-3300-6; d) 100-count bottles, NDC 64727-3300-1; and e) 1,000-count bottles, NDC 64727-3300-2; Rx only, Manufactured by: RLC Labs Phoenix, AZ 85034.
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