KABANA SKIN CARE: Drug Recall
Recall #D-0513-2025 · 03/12/2025
Class II: Risk
Recall Details
- Recall Number
- D-0513-2025
- 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
- 54 tubes
Reason for Recall
cGMP deviations
Product Description
Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen, Broad Spectrum SPF 32, 25% Zinc Oxide, 3 FL OZ/ 85 mL per bottle, Made in USA for Erin's Faces, Millburn, NO 07041. NDC: 73369-1401-1
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.