D-0513-2025 Class II Ongoing

Recalled by KABANA SKIN CARE — Louisville, CO

FDA drug recall D-0513-2025 was initiated by KABANA SKIN CARE on March 12, 2025 and is designated Class II. Reason for recall: cGMP deviations The recall status is ongoing. Affected quantity: 54 tubes.

Recall Details

Product Type
Drugs
Report Date
July 16, 2025
Initiation Date
March 12, 2025
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
54 tubes

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

Reason for Recall

cGMP deviations

Distribution Pattern

NJ, FL, MI

Code Information

Lot: 410-002