Iowa Select Herbs Recalls Acia Berry Supplement Due to Misbranding
Iowa Select Herbs LLC is recalling 10 bottles of Acia Berry dietary supplement because the product is misbranded, an unapproved new drug, and an adulterated supplement.
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 hazards involve regulatory violations (misbranding, adulteration) rather than immediate physical injury or high-risk pathogens.
Plain-English summary
Iowa Select Herbs LLC is recalling 10 bottles of Acia Berry (Euterpe oleracea) dietary supplement, 4 fl. Oz. (120 ml) size. The 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.
The recall is being conducted pursuant to a consent decree for injunctive relief. The firm was ordered to recall the products because they are misbranded, unapproved new drugs, and adulterated dietary supplements. The specific lot number is 22345, with an expiration date of 05/2017.
Consumers who have purchased this product should stop using it and contact the recalling firm for further instructions.
The recalled product
- Product
- Iowa Select Herbs LLC, Acia Berry (Euterpe oleracea), www.iowaselectherbs.com, 4 fl. Oz. (120 ml), Cedar Rapids, IA 52402
- Manufacturer
- Iowa Select Herbs LLC
- Category
- Food — Dietary Supplement
- Affected units
- 10
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 - 22345
- Expires 05/2017
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
Same manufacturer · Iowa Select Herbs LLC
See all →- ModerateIowa Select Herbs Recalls Reishi Mushroom Product Due to Misbranding
FDA (Food) · 2016-05-11
- ModerateIowa Select Herbs Recalls Kava Kava Root for Misbranding and Adulteration
FDA (Food) · 2016-05-11
- ModerateIowa Select Herbs Recalls Damiana Leaf Due to Misbranding and Adulteration
FDA (Food) · 2016-05-11
- ModerateIowa Select Herbs Recalls Dandelion Root for Misbranding and Adulteration
FDA (Food) · 2016-05-11
- ModerateIowa Select Herbs Recalls Chaparral Leaf Due to Misbranding and Adulteration
FDA (Food) · 2016-05-11
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02