KABANA SKIN CARE recalls specific sunscreen products for manufacturing quality issues. Affected items include GreenScreen, Bread Spectrum, and Zinc Ox: 3.4 fl oz tubes with NDC 73369-0001-1. Consumers should check labels and contact the company.
cGMP deviations
KABANA SKIN CARE is recalling several sunscreen products due to manufacturing quality deviations. This means the products may not meet safety standards, and using them could pose risks.
The recall is for 'cGMP deviations,' which means the products did not meet current Good Manufacturing Practices. This could affect the product's safety and quality, but the exact risk is not specified in the recall notice.
People who own or use KABANA SKIN CARE sunscreens with the specific product names and NDC numbers listed. Those with sensitive skin or children may be at higher risk due to the product's 'Baby Safe' claim.
Check for the product names: GreenScreen, Bread Spectrum UVA & UVB, Zinc Oxide Sunscreen, or the NDC number 73369-0001-1 on the tube. The product comes in 3.4 fl oz tubes labeled as 'Baby Safe.'
Look for the NDC number 73369-0001-1 or the product names listed in the recall notice.
The recall is for 'cGMP deviations,' which means the products did not meet current Good Manufacturing Practices. The exact risk is not specified in the recall notice.
The recall notice does not provide a specific remedy, so check the product labels and contact KABANA SKIN CARE for further instructions.
The recall notice does not specify the risk level or potential injuries, so the danger level is unknown.
We’ve drafted a message you can send KABANA SKIN CARE to request your refund or repair — edit it as you like.
Subject: Recall D-0514-2025 — KABANA SKIN CARE KABANA SKIN CARE Hello, I own a KABANA SKIN CARE that is covered by recall D-0514-2025 from KABANA SKIN CARE. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
