B Natural Organics, Organic Sunscreen, Broad Spectrum, SPF 30, 25% non-nano Zinc Oxide, a) Nude Tint Mineral Formula for
Summary
The FDA issued a Class II for B Natural Organics, Organic Sunscreen, Broad Spectrum, SPF 30, 25% non-nano Zinc by KABANA SKIN CARE. Reason: cGMP deviations.
Details
Source
Drug Recall
External ID
D-0512-2025
Action Date
2025-07-16
Status
Ongoing
Category
drug
Product Description
B Natural Organics, Organic Sunscreen, Broad Spectrum, SPF 30, 25% non-nano Zinc Oxide, a) Nude Tint Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1002-2; b) Tint Free Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1001-2; c) Tan Tint Mineral Formula for Face and Body, 4 oz. (120 ML) per bottle. NDC: 73369-1003-2.
Lot/Code Info: Lots: a) 410-001, Exp 10/31/2027 b) 404-003, Exp 04/30/2027 c) 404-001, Exp 04/30/2027
Quantity Affected: 204 tubes
Reason for Recall
cGMP deviations
Distribution
NJ, FL, MI
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-12
Company
Louisville, CO
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 89 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.
KABANA SKIN CARE has 4 FDA actions in our database, including 4 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (KABANA SKIN CARE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does KABANA SKIN CARE have FDA actions?
KABANA SKIN CARE has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "D-0512-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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