Kingskin Liquid
FDA Recall NDC 55758-409
FDA Enforcement Report: View Recall Date, Reasons, and Safety Status
Active & Historical Enforcement Reports
The FDA has identified 1 recorded enforcement report(s) associated with Kingskin (NDC 55758-409). A significant event, classified as Class II, was initiated on Apr 15, 2025 by Pharmadel Llc. The reported reason for this action was: "cGMP deviations"
This specific recall has a current status of TERMINATED, indicating that the FDA considers the recall process finished or the product successfully recovered.
This specific recall has a current status of TERMINATED, indicating that the FDA considers the recall process finished or the product successfully recovered.
Reported Recall Events
Class II Terminated
cGMP deviations
Apr 15, 2025
Apr 30, 2025
20,048 bottles
Recall Profile & Regulatory Data
Event ID
96639
Classification
Class II
Enforcement Status
Terminated
Recalling Firm
Pharmadel, LLC
Voluntary / Mandated
Voluntary: Firm initiated
Distribution Pattern
DE
Termination Date
Jan 08, 2026
Product Description
Kingskin, Elimina Las Verrugas, For the removal of common warts, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-409-15
Batch or Lot Expiration Information
Lot# Lot, expiry: KSE-01, EXP: OCT 26; KSE-02, EXP: FEB 27
Affected Packages Involved in this Recall
55758-409-15Product
About FDA Recall Enforcement Reports
FDA recall data documents classified recall actions associated with a product. Most recalls are limited to specific lots, batches, or package configurations rather than every unit of a drug.
If a recall is listed for an NDC, review the affected lot information and package details carefully. Patients and healthcare professionals should confirm whether a specific product in hand matches the lot or package information before assuming it is affected.
