Dermanak original crema blanqueador Skin Fade Cream recalled over manufacturing violations
- Recall date
- June 21, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Pharma-Natural Inc. recalls Dermanak original crema blanqueador (Hydroquinone 2%) Skin Fade Cream, 2 OZ. (56.7 g) jar, Manufactured by: Pamby Distr…
- Recall number
- D-1500-2019
- FDA classification
- Class II
- Brand / firm
- Pharma-Natural Inc.
- Sold / distributed
- Consignees in FL and TX who may have further distributed Nationwide in the USA and Puerto Rico.
Why it was recalled
CGMP Deviations: products were manufactured with lack of process validation, cleaning validation, stability studies, and other current good manufacturing practice violations.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Dermanak original crema blanqueador (Hydroquinone 2%) Skin Fade Cream, 2 OZ. (56.7 g) jar, Manufactured by: Pamby Distributors, Inc., Miami, FL 33126, NDC 63788-108-02.
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