RecallHawk
Class II Recall

Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen, Broad Spectrum SPF 32, 25% Zinc Oxide, 3 FL OZ/ 85 mL per bottle, Made

KABANA SKIN CARE

Summary

The FDA issued a Class II for Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen, Broad Spectrum SPF 32, 25% Zinc by KABANA SKIN CARE. Reason: cGMP deviations.

Details

Source

Drug Recall

External ID

D-0513-2025

Action Date

2025-07-16

Status

Ongoing

Category

drug

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

Lot/Code Info: Lot: 410-002

Quantity Affected: 54 tubes

Reason for Recall

cGMP deviations

Distribution

NJ, FL, MI

Type: Voluntary: Firm initiated

Recall Initiated: 2025-03-12

Company

KABANA SKIN CARE

Louisville, CO

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 89 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

KABANA SKIN CARE has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (KABANA SKIN CARE) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does KABANA SKIN CARE have FDA actions?

KABANA SKIN CARE has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0513-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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