Aveeno Daily Moisturizing Lotion recalled due to improper storage conditions
Family Dollar and Johnson & Johnson Consumer are recalling Aveeno Daily Moisturizing Lotion due to cGMP violations involving improper storage temperature. No illnesses have been reported.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: This is an FDA Class II recall for a manufacturing/storage process deviation with no reported illnesses, injuries, or confirmed contamination. Precautionary recalls without specific health hazards or reported harm are classified as Moderate.
Plain-English summary
Aveeno Daily Moisturizing Lotion Fragrance Free with Soothing Oat & Rich Emollients (5 oz, 141 g, SKU 2005444) is being recalled. The product was distributed by Johnson & Johnson Consumer, Inc. (Skillman, NJ).
The lotion is being recalled due to current Good Manufacturing Practice (cGMP) deviations. Specifically, the product was stored outside of the temperature range specified on its label, which may affect product quality and stability.
The affected lotion was distributed nationwide. No illnesses or injuries have been reported related to this product. Consumers who have purchased this lotion should discontinue use and contact their retailer for information regarding refunds or product disposal.
The recalled product
- Product
- Aveeno Daily Moisturizing lotion Fragrance Free with Soothing Oat & Rich Emollients, Net Wt. 5 oz (141 g), Distributed by Johnson & Johnson Consumer, Inc. Skillman, NJ 08558, UPC 3 81137-001530 7
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Drug — Skincare
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- SKUs 2005444
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 7 recalled by Family Dollar Stores, Llc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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