KABANA SKIN CARE: Drug Recall
Recall #D-0515-2025 · 03/12/2025
Class II: Risk
Recall Details
- Recall Number
- D-0515-2025
- 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
- 76 bottles
Reason for Recall
cGMP deviations
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
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.