Hand Sanitizer Recall: Storage Temperature Non-Compliance at Family Dollar
Family Dollar Stores is recalling Luxury Hygiene Hand Sanitizer Moisturizing Formula due to cGMP deviations related to improper storage outside labeled temperature requirements.
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: FDA Class II recall for a storage and cGMP deviation. The hazard—potential loss of product efficacy from improper storage—is precautionary in nature, with no documented illnesses or injuries mentioned in the source material. Precautionary storage-based recalls without confirmed health impacts are classified as Moderate.
Plain-English summary
Family Dollar Stores, LLC is recalling Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E (8 FL. OZ. / 236 mL) distributed nationwide. The recalled product was stored outside of its labeled temperature requirements during manufacturing, a cGMP deviation.
Improper storage conditions can compromise the efficacy of hand sanitizer, potentially affecting its ability to eliminate bacteria and viruses from hands. The product was distributed under SKU 2007626.
Consumers who have purchased this product should discontinue use and contact Family Dollar Stores for information on product returns or disposal.
The recalled product
- Product
- Luxury Hygiene Hand Sanitizer Moisturizing Formula with Vitamin E, 8 FL. OZ. (236 mL), TSM Brands LLC 540 Equinox Ln Manalapan, NJ 07726, UPC 6 86275 96536 9
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Drug — Hand Sanitizer
- Hazard
- improper-storage
- efficacy-loss
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 2007626
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- CriticalWarfarin Tablets Recalled After Mix-Up Between 2.5 mg and 5 mg Strengths
FDA (Drugs) · 2026-07-21
- ModerateFDA Recalls Pred Mild Ophthalmic Suspension Due to Failed Stability Specifications
FDA (Drugs) · 2026-06-03
- ModerateNicotine Transdermal System Patches Recalled for Oxidative Impurity Specification Failure
FDA (Drugs) · 2026-06-03
- LowPrimidone Tablets Recalled Due to Cross-Contamination with Acemetacin
FDA (Drugs) · 2026-05-27
- HighLiraglutide Injection Recalled Due to Particulate Matter in Cartridges
FDA (Drugs) · 2026-05-27