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Use caution Drug recall · FDA · Published July 25, 2018

Recall: alba BOTANICA Sensitive Sheer Shield Sunscreen Microbial Contamination

The Hain Celestial Group recalls specific lots of alba BOTANICA sunscreen due to microbial contamination. Check your tube's lot code and UPC.

🇺🇸 FDA recall #D-1078-2018Drugalba BOTANICA ›
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Recalling firmThe Hain Celestial Group, Inc. - Worldwide HQ1111 Marcus Ave · New Hyde Park, NY 11042-1221
✎ GovInfoNow plain-language explainer

What happened, in plain English

The Hain Celestial Group, Inc. is recalling one lot of alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free SPF 50+ because it contains microbial contamination. This product was distributed to a distributor in California, which may have shared it further within the U.S. The recall involves 1,098 tubes manufactured by The Hain Celestial Group. Read more at govinfonow.com/recall/39856-recall-alba-botanica-sensitive-sheer-shield-sunscreen-microbial-contamination.

Source Summary by GovInfoNow · govinfonow.com/recall/39856-recall-alba-botanica-sensitive-sheer-shield-sunscreen-microbial-contamination · Updated October 11, 2026 · FDA enforcement record: FDA #D-1078-2018

Cite this page

“Recall: alba BOTANICA Sensitive Sheer Shield Sunscreen Microbial Contamination.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/39856-recall-alba-botanica-sensitive-sheer-shield-sunscreen-microbial-contamination. 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 product is classified as a non-sterile item that has been found to have microbial contamination. While the record does not specify exact injuries, contaminated topical products can pose health risks if used on the skin.

Who’s affected

Consumers who purchased alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free SPF 50+ from a distributor in California are affected. Individuals using this specific non-sterile sunscreen may be at risk due to the microbial contamination.

How to tell if you have this one

Check your sunscreen tube for the UPC 7 24742 00438 5 and Lot code 8041. The product is an 85 g (3 oz) tube of alba BOTANICA Sensitive Sheer Shield Sunscreen Fragrance Free SPF 50+.

  • 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

Where it went and when

Where it was distributed

Distributed in California.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: yesCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Product was distributed to one distributor in California who may have distributed the product further within the US.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: California.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Jul 25, 201812. FDA classified it Class II: Aug 14, 201823. Published in FDA’s Enforcement Report: Aug 22, 201834. FDA terminated the recall: Jan 18, 2019420182019
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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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 qwen3.6:35b-a3b on October 11, 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