Advil Ibuprofen Tablets Recalled for Storage Temperature Deviation
Family Dollar Stores is recalling Advil Ibuprofen 200 mg tablets due to a storage temperature deviation during manufacturing and distribution. 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 with no reported illnesses or injuries. The hazard is a CGMP storage temperature deviation that could affect product quality, but without evidence of actual harm, it qualifies as a precautionary recall.
Plain-English summary
Family Dollar Stores, Llc. is recalling Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer, in three packaging formats: 100-count bottles, 50-count bottles, and multi-packs of 3 packets (2 tablets per packet). The recalled product was distributed nationwide between July 28, 2022 and March 31, 2023.
The recall stems from a Current Good Manufacturing Practice (CGMP) deviation: the product was stored and distributed outside the labeled storage temperature requirements during the manufacturing and distribution process.
No illnesses or injuries have been reported in connection with this recall. Consumers with the recalled product should stop using it.
The recalled product
- Product
- Advil Ibuprofen Tablets, 200 mg Pain Reliever/Fever Reducer (NSAID) packaged in a) 100-count bottles, b) 50-count bottles, and c) 3 (2 count) packets.
- Manufacturer
- Family Dollar Stores, Llc.
- Category
- Drug — Pain Reliever
- 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 (3)
- SKUs a) 0901458
- b) 0913023
- c) 0999259 stored and distributed from DCs 07/28/2022 through 03/31/2023.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 4 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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