# FDA recall D-0512-2025

> **KABANA SKIN CARE** · Class II · drug recall initiated 2025-03-12.

## Product

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.

## Reason for recall

cGMP deviations

## Distribution

NJ, FL, MI

## Key facts

- **Recall number:** D-0512-2025
- **Recalling firm:** KABANA SKIN CARE
- **Classification:** Class II
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2025-03-12
- **Report date:** 2025-07-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Louisville, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0512-2025

## Citation

> AI Analytics. FDA recall D-0512-2025. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/D-0512-2025. Source: US FDA. Licensed CC0.

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