Taro Recalls Kroger Clotrimazole Cream Due to Impurity
Taro Pharmaceuticals is recalling Kroger Athlete's Foot Cream because an unknown degradation impurity was detected slightly above the specification limit.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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: The recall is classified as FDA Class II, and the hazard involves an impurity detected slightly above the specification limit without reported injuries, fitting the criteria for a moderate severity recall.
Plain-English summary
Taro Pharmaceuticals U.S.A., Inc. is recalling 133,452 tubes of Kroger Athlete's Foot Cream, Clotrimazole Cream USP, 1%. The product is an over-the-counter antifungal cream distributed nationwide in the USA and Canada.
The recall was initiated because an unknown degradation impurity was detected slightly above the specification limit in the product. The affected lots are A873430372 (Expiration: Dec 2020) and D867331278 (Expiration: Mar 2021).
Consumers should stop using the recalled product and return it to the place of purchase for a refund or contact Taro Pharmaceuticals for further information.
The recalled product
- Product
- KROGER (CLOTRIMAZOLE)
- Brand
- KROGER
- Manufacturer
- Taro Pharmaceuticals U.S.A., Inc.
- Category
- Drug — Topical Antifungal
- 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 (4)
- Lot#: A873430372
- Exp Dec 2020
- D867331278
- Exp Mar 2021
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 10 recalled by Taro Pharmaceuticals U.S.A., Inc. 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.
See all 10 products in this recall →Related recalls
Same brand · KROGER
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FDA (Drugs) · 2020-12-23
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