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Drug recall · FDA · Published July 25, 2018

The Hain Celestial Group, Inc. - Worldwide HQ recalls alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free spf 50+ , 85 g 3 oz tube. Manufactured by: The Haine

alba BOTANICA Sensitive Sheer Shield Sunscreen (SPF 50+) with microbial contamination risk. Recalled due to potential health hazards from non-sterile product. Consumers should check UPC 7 24742 00438 5 and lot code 8041.

🇺🇸 FDA recall #D-1078-2018Drugalba BOTANICA ›
Take action

Contact the company & request your remedy

Recalling firmThe Hain Celestial Group, Inc. - Worldwide HQ1111 Marcus Ave · New Hyde Park, NY 11042-1221
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

alba BOTANICA Sensitive Sheer Shield Sunscreen (SPF 50+) is being recalled because it may contain microbial contamination. This poses a health risk as the product is not sterile, potentially causing infections or other health issues if used. Read more at govinfonow.com/recall/39856-alba-botanica-sensitive-sheer-shield-sunscreen-microbial-contamination-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/39856-alba-botanica-sensitive-sheer-shield-sunscreen-microbial-contamination-hazard · Updated October 6, 2026 · FDA enforcement record: FDA #D-1078-2018

Cite this page

“alba BOTANICA Sensitive Sheer Shield Sunscreen: Microbial Contamination Hazard.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/39856-alba-botanica-sensitive-sheer-shield-sunscreen-microbial-contamination-hazard. Based on FDA recall #D-1078-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1078-2018%22&limit=1).

Why it’s dangerous

The sunscreen product is not sterile and may contain harmful microorganisms. This contamination could lead to skin infections or other health problems, especially for individuals with sensitive skin or compromised immune systems.

Who’s affected

Anyone who owns or uses the recalled sunscreen. People with sensitive skin or those prone to infections may be at higher risk due to the non-sterile nature of the product.

How to tell if you have this one

Check for the product name 'alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free spf 50+', 85g tube. Look for UPC 7 24742 00438 5 and lot code 8041 on the packaging.

  • Brand
    alba BOTANICA
  • Product
    alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free spf 50+ , 85 g 3 oz tube. Manufactured by: The Haine
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Identify the product by UPC 7 24742 00438 5 and lot code 8041 on the tube.

✎ GovInfoNow

Questions people ask

Is this sunscreen safe to use?

The recall indicates potential microbial contamination, so it is not safe to use. The product is non-sterile and may cause health issues.

How can I check if I have the recalled product?

Look for the UPC 7 24742 00438 5 and lot code 8041 on the product packaging.

What should I do if I have the recalled sunscreen?

The recall does not specify a remedy, so contact the manufacturer for further instructions.

Take action

Contact alba BOTANICA

We’ve drafted a message you can send alba BOTANICA to request your refund or repair — edit it as you like.

Subject: Recall D-1078-2018 — alba BOTANICA alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free spf 50+ , 85 g 3 oz tub

Hello,

I own a alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free spf 50+ , 85 g 3 oz tube. Manufactured by: The Haine that is covered by recall D-1078-2018 from alba BOTANICA.

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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Where this comes from

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.

  • Official source: FDA Recall #D-1078-2018 (July 25, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1078-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA