PlainRecalls
FDA Drug Moderate Class II Ongoing

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.

Reported: May 28, 2025 Initiated: April 24, 2025 #D-0428-2025

Product Description

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.

Reason for Recall

CGMP Deviations

Details

Units Affected
10,000 Tubes
Distribution
DE and NC
Location
Ta. Kadi, District Mehsana, N/A

Frequently Asked Questions

What product 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.. Recalled by KENIL HEALTHCARE PRIVATE LIMITED. Units affected: 10,000 Tubes.
Why was this product recalled?
CGMP Deviations
Which agency issued this recall?
This recall was issued by the FDA Drug on May 28, 2025. Severity: Moderate. Recall number: D-0428-2025.