FDA recall record

KABANA SKIN CARE In Your Face Mineral Tint SPF 31, Zinc Oxide 25%, Tinted Sunscreen Broad recall — FDA D-0515-2025

cGMP deviations

Class IIclassification
D-0515-2025official record ID
Jul 16, 2025report date

Recall record at a glance

Official recordD-0515-2025
CategoryDrug Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmKABANA SKIN CARE
Report dateJul 16, 2025
Recall initiation dateMar 12, 2025
Quantity76 bottles
LocationLouisville, CO, United States

Official product description

In Your Face Mineral Tint SPF 31, Zinc Oxide 25%, Tinted Sunscreen Broad Spectrum UVA & UVB chemical free, Organic Ingredients, Biodegradable & Baby Safe, 50 mL - 1.7 fl oz per bottle, Manufactured for IN YOUR FACE Skin Care, Belleair Bluffs, FL, Made in USA, NDC: 73369-1601-1

Why the product was recalled

cGMP deviations

Distribution information

NJ, FL, MI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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