Iowa Select Herbs Recalls Saw Palmetto Berry Due to Misbranding and Adulteration
Iowa Select Herbs LLC is recalling Saw Palmetto Berry products 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 is defined as unlikely to cause adverse health consequences, aligning with the Moderate severity score for minor labeling or regulatory issues.
Plain-English summary
Iowa Select Herbs LLC is recalling specific bottles of Saw Palmetto Berry (Serenoa repens) in 4 fl. Oz., 16 fl. Oz., 32 fl. Oz., and unknown sizes. The recalled product is identified by Lot-32654 with an expiration date of 09/2019.
The recall is being conducted pursuant to a consent decree for injunctive relief, which ordered the firm to recall all products because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
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 further instructions.
The recalled product
- Product
- Iowa Select Herbs LLC, Saw Palmetto Berry (Serenoa repens), www.iowaselectherbs.com, (a) 4 fl. Oz. (b) 16 fl. Oz., (c) 32 fl. Oz., (d) unknown size., Cedar Rapids, IA 52402
- Manufacturer
- Iowa Select Herbs LLC
- Category
- Food — Dietary Supplement
- 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 (1)
- Lot-32654 Expires-09/2019
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.
See all 104 products in this recall →Related recalls
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