First Aid Beauty has announced the recall of 2,756 jars of its Ultra Repair Cream in the coconut vanilla scent following an issue identified by the brand.

First Aid Beauty recalled more than 2,000 jars of a “specific variant” of a moisturizing cream and said no other versions were affected.

The FDA has given the recall of the coconut vanilla version of Ultra Repair Cream its second-highest risk classification. Here's what that means.

Last month, nearly 3,000 jars of First Aid Beauty Ultra Repair Cream were recalled nationwide because a batch "intended for quarantine" was accidentally sold, the FDA said.

The popular skincare brand First Aid Beauty, known for its gentle and hydrating formulas, has issued a voluntary product recall. The brand released over 2,500 jars of their 14-ounce Ultra Repair Cream in the coconut vanilla scent,

First Aid Beauty has recalled nearly 2,800 jars of 14 oz. Ultra Repair Cream Coconut Vanilla moisturizer. According to the company, the products were “inadvertently sold,” and were “not intended for market sale.” The recall covers only Ultra Repair Cream Coconut Vanilla sold directly via FirstAidBeauty.com in the U.S.

First Aid Beauty has issued a recall for 2,756 14-ounce jars of its Ultra Repair Cream, colloidal oatmeal 0.5% Coconut Vanilla. According to the U.S. Food

First Aid Beauty is recalling its Ultra Repair Cream Coconut Vanilla. The moisturizer was not meant to be sold to consumers. Approximately 2,756 jars were sold online in the United States.

The First Aid Beauty ‘Ultra Repair Intense Hydration’ cream is typically a well-loved product that has previously gone viral on TikTok but now, users feel as if they’re being left in the dark

Users of First Aid Beauty, a skin care company based out of Massachusetts, learned of the voluntary recall in December when the company realized it had sent out more than 2,700 containers of the 4-ounce Ultra Repair Cream Coconut Vanilla.

"This product was not intended for market sale," First Aid Beauty noted in a statement on its website. The FDA added the recall was due to a "Current Good Manufacturing Practice deviation," which doesn't necessarily mean there is anything wrong with the product.