Johnson & Johnson recalls Neutrogena Ultra Sheer body mist sunscreen due to cGMP deviations. Affected units may pose quality risks; contact for return instructions.
cGMP Deviations
Johnson & Johnson is recalling Neutrogena Ultra Sheer body mist sunscreen SPF 30 because of manufacturing quality issues. This recall does not involve immediate safety risks but requires consumers to return the product to avoid potential quality problems.
The product was manufactured under cGMP (Current Good Manufacturing Practice) deviations, which means the production process did not meet quality standards. This could lead to inconsistent product performance or quality issues, but it does not pose a direct health risk.
All owners of Neutrogena Ultra Sheer body mist sunscreen SPF 30 with the described ingredients and UPC 0 86800 11133 7 are affected. People who use sunscreen regularly are most at risk of receiving the recalled product.
Check for the product name 'Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30' with ingredients Avobenzone (3%), Homosalate (8%), Octisalate (5%), Octocrylene (8%), and net weight 8.0 oz. (226 g). The product was distributed by Johnson & Johnson Consumer, Inc. with UPC 0 86800 11133 7.
Verify the product name, ingredients, and UPC code to confirm if it matches the recalled item.
Contact Johnson & Johnson Consumer, Inc. to return the product for a refund or replacement.
The recall is due to manufacturing quality issues, not safety risks. The product is safe to use but should be returned per the recall instructions.
Check for the product name 'Neutrogena Ultra Sheer body mist sunscreen BROAD SPECTRUM SPF 30' with the specified ingredients and UPC 0 86800 11133 7.
Contact Johnson & Johnson Consumer, Inc. to return the product for a refund or replacement.
We’ve drafted a message you can send Neutrogena to request your refund or repair — edit it as you like.
Subject: Recall D-0847-2021 — Neutrogena Neutrogena Hello, I own a Neutrogena that is covered by recall D-0847-2021 from Neutrogena. 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.
