Iowa Select Herbs Recalls Olive Leaf Supplements Due to Misbranding
Iowa Select Herbs LLC is recalling Olive Leaf dietary supplements because they are misbranded, unapproved new drugs, and adulterated.
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 recall is classified as FDA Class III, which indicates the product is unlikely to cause adverse health consequences. The issues are regulatory (misbranding, unapproved new drug status, adulteration) rather than acute physical hazards like choking or high-risk pathogens.
Plain-English summary
Iowa Select Herbs LLC is recalling Olive Leaf (Olea europa) dietary supplements in various sizes, including 4 fl. oz., 16 fl. oz., and 1 gallon bottles. 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 32772, with an expiration date of 05/2019.
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 contact the manufacturer for instructions on disposal or return.
The recalled product
- Product
- Iowa Select Herbs LLC, Olive Leaf (Olea europa), www.iowaselectherbs.com, (a) 4 fl. Oz. (b) 16 fl. Oz., (c) 1 gallon (d) Unknown size. Cedar Rapids, IA 52402
- Manufacturer
- Iowa Select Herbs LLC
- Category
- Food — Dietary Supplements
- 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 (2)
- Lot - 32772
- Expires - 05/2019
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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