CLASS II ONGOING Drug recall · Reported 16 Jul 2025 · FDA Enforcement Report

Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen recalled

Kabana Skin Care is recalling Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen, Broad Spectrum SPF 32, 25% Zinc Oxide per, distributed in Florida, Michigan, New Jersey. The recall was initiated on 12 Mar 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: 410-002
Quantity recalled54 tubes

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0513-2025
FDA event ID
96853
Recalling firm
Kabana Skin Care, Louisville, CO
Classification
Class II
Status
Ongoing
Recall initiated
12 Mar 2025
FDA classified
10 Jul 2025
Reported
16 Jul 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

12 Mar 2025Recall initiated by company
10 Jul 2025Classified by FDA+120 days
16 Jul 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

cGMP deviations

Product as listed by the FDA

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

Where it was distributed

NJ, FL, MI

FloridaMichiganNew Jersey

Questions about this recall

Is Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen, Broad Spectrum SPF 32, 25% Zinc Oxide per recalled?

Yes. Kabana Skin Care recalled Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen, Broad Spectrum SPF 32, 25% Zinc Oxide per on 12 Mar 2025. The recall is Class II and its status is Ongoing. Recall number D-0513-2025.

Why was it recalled?

cGMP deviations

Which lots are affected?

Lot: 410-002

Where was it sold?

NJ, FL, MI

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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