KABANA SKIN CARE: Drug Recall

Recall #D-0514-2025 · 03/12/2025

Class II: Risk

Recall Details

Recall Number
D-0514-2025
Classification
Class II
Product Type
Drug
Recalling Firm
KABANA SKIN CARE
Status
Ongoing
Date Initiated
03/12/2025
Location
Louisville, CO, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
174 tubes

Reason for Recall

cGMP deviations

Product Description

GreenScreen, kabana organic skincare, Bread Spectrum UVA & UVB, Zinc Oxide Sunscreen, Organic Ingredients, Fragrance Free, Biodegradable, Chemical Free, Non-Nano, Baby Safe, Original, SPF 32, Totally Green personal care, Zinc Oxide USP 25%, 3.4 FL OZ/115 G Tube, NDC: 73369-0001-1

Distribution Pattern

NJ, FL, MI

Other Recalls by KABANA SKIN CARE

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Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.