Iowa Select Herbs Recalls Acerola Berry Supplement Due to Misbranding
Iowa Select Herbs LLC is recalling 10 bottles of Acerola Berry (Malpighia) liquid supplement because the product is misbranded, an unapproved new drug, and an adulterated dietary supplement.
The agency’s classification
FDA (Food): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
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 III, which indicates the product is unlikely to cause adverse health consequences. The hazards involve regulatory violations (misbranding, adulteration) rather than acute physical injury risks like choking or fire.
Plain-English summary
Iowa Select Herbs LLC is recalling 10 bottles of 4 fl. oz. (120 ml) Acerola Berry (Malpighia) liquid supplement. The product was manufactured in Cedar Rapids, IA, and carries Lot 32795 with an expiration date of 04/2019.
The recall was initiated 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 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 who purchased this product should stop using it and return it to the place of purchase for a refund or contact the recalling firm for further instructions.
The recalled product
- Product
- Iowa Select Herbs LLC, Acerola Berry (Malpighia), www.iowaselectherbs.com, 4 fl. Oz. (120 ml), Cedar Rapids, IA 52402
- Manufacturer
- Iowa Select Herbs LLC
- Category
- Food — Dietary Supplement
- Hazard
- 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 - 32795
- Expires 04/2019
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
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 →- ModerateEl Ruisenor De Mexico Recalls Soybeans for Undeclared Soy Allergen
FDA (Food) · 2026-10-28
- ModerateEl Ruisenor De Mexico Recalls Textured Soy Protein for Undeclared Soy
FDA (Food) · 2026-10-28
- ModerateEl Ruisenor De Mexico Recalls Black Sesame Seeds for Undeclared Allergen
FDA (Food) · 2026-10-28
- ModerateEl Ruisenor De Mexico Recalls Wheat Bran for Undeclared Wheat Allergen
FDA (Food) · 2026-10-28
- ModerateEl Ruisenor De Mexico Recalls Ground Shrimp for Undeclared Allergen
FDA (Food) · 2026-10-28
Similar recalls
- ModerateBaby Allergy herbal supplement recalled over unapproved drug claims and misbranding
FDA (Food) · 2025-12-31
- ModerateMullein ear drops recalled over unapproved drug claims and missing supplement facts
FDA (Food) · 2025-12-31
- ModeratePain Away herbal supplement recalled over unapproved drug claims and misbranding
FDA (Food) · 2025-12-31
- ModerateHerbal Doctor Remedies Recalls Metabolic Booster Capsules for Misbranding
FDA (Drugs) · 2020-04-15
- ModerateChaga mushroom supplement recalled over unapproved drug claims and misbranding
FDA (Food) · 2025-12-31
- ModerateHerbal Doctor Remedies Recalls Sugar Off Capsules Due to Misbranding
FDA (Drugs) · 2020-04-15