FindMyRecallSubscribe
Class II: temporary or reversible health riskOngoing

Kabana Skin Care Erin's Faces Recall

Erin's Faces, Mineral SPF 32, UVA/UVB Sunscreen, Broad Spectrum SPF 32, 25% Zinc Oxide,…

KABANA SKIN CARE · Louisville, CO

Risk level
Class II
Reported by FDA
Jul 16, 2025
Recall ID
D-0513-2025
Check your lot numberHow we source this data

Summary

Kabana Skin Care recalled Erin's Faces starting Mar 12, 2025. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report D-0513-2025 on Jul 16, 2025. Reason: cGMP deviations. Status: Ongoing.

Why it was recalled

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

Lot numbers, UPCs & expiration codes

Lot: 410-002

Where it was sold

NJ, FL, MI

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0513-2025
Classification
Class II
Status
Ongoing
Recall initiated
Mar 12, 2025
FDA report date
Jul 16, 2025
Quantity
54 tubes
Recall type
Voluntary: Firm initiated
Recalling firm
KABANA SKIN CARE

Original FDA data

Every field from FDA enforcement report D-0513-2025, exactly as published.

Show all FDA fields
City
Louisville
State
CO
Status
Ongoing
Country
United States
Event ID
96853
Address
685 S Arthur Ave Unit 9b
Code information
Lot: 410-002
Postal code
80027-3141
Report date
Jul 16, 2025
Product type
Drugs
Recall number
D-0513-2025
Classification
Class II
Recalling firm
KABANA SKIN CARE
Product quantity
54 tubes
Reason for recall
cGMP deviations
Voluntary / mandated
Voluntary: Firm initiated
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
Recall initiation date
Mar 12, 2025
Initial firm notification
Letter
Center classification date
Jul 10, 2025

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0513-2025, published Jul 16, 2025. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

How we source and update recall data · Report incorrect information

Other recent drug recalls