KABANA SKIN CARE: Drug Recall
Recall #D-0512-2025 · 03/12/2025
Class II: Risk
Recall Details
- Recall Number
- D-0512-2025
- 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
- 204 tubes
Reason for Recall
cGMP deviations
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.
Distribution Pattern
NJ, FL, MI
Other Recalls by KABANA SKIN CARE
- Class II: Risk 03/12/2025
- Class II: Risk 03/12/2025
- Class II: Risk 03/12/2025
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.