Iowa Select Herbs Recalls Ginkgo Biloba for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling Ginkgo biloba products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
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: The agency classification is FDA Class III, which the rubric indicates are typically scores of 1 or 2 as they are unlikely to cause adverse health consequences. The recall is driven by regulatory status (misbranding/adulteration) rather than reported acute injuries.
Plain-English summary
Iowa Select Herbs LLC is recalling Ginkgo Leave (Ginkgo biloba) products, 7.5 fl. Oz. bottles, manufactured in Cedar Rapids, IA. The recall is being conducted pursuant to a consent decree for injunctive relief.
The FDA determined that the recalled products are misbranded, unapproved new drugs, and adulterated dietary supplements. The specific lot number is 30520, with an expiration date of 08/2018.
The recalled product was distributed to retail stores in California, Florida, Georgia, Iowa, Michigan, Missouri, Montana, New York, and South Carolina, as well as to consumers nationwide and internationally in Denmark, Canada, the UK, Australia, and Serbia. Consumers should stop using the product and follow the instructions provided by the recalling firm or the FDA.
The recalled product
- Product
- Iowa Select Herbs LLC, Ginkgo Leave (Ginkgo biloba), www.iowaselectherbs.com, 7.5 fl. Oz., Cedar Rapids, IA 52402
- Manufacturer
- Iowa Select Herbs LLC
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 1
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 (2)
- Lot - 30520
- Expires - 08/2018
Distribution
Part of a larger recall action
This product is one of 104 recalled by Iowa Select Herbs LLC under a single FDA (Food) 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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