Rapidol Maximum Strength recalled over manufacturing violations
- Recall date
- April 24, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- KENIL HEALTHCARE PRIVATE LIMITED recalls Rapidol Maximum Strength, Hydrocortisone 1% Anti-Itch Cream, NET WT 2 oz (60g) Tube, Distributed by: Pharmadel LLC, New…
- Recall number
- D-0428-2025
- FDA classification
- Class II
- Brand / firm
- KENIL HEALTHCARE PRIVATE LIMITED
- Sold / distributed
- DE and NC
Why it was recalled
CGMP Deviations
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Rapidol Maximum Strength, Hydrocortisone 1% Anti-Itch Cream, NET WT 2 oz (60g) Tube, Distributed by: Pharmadel LLC, New Castle, DE, 19720, NDC 55758-420-02, UPC 8 10096 77158 2.
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