Iowa Select Herbs Recalls Artichoke Leaf Extract for Misbranding and Adulteration
Iowa Select Herbs LLC is recalling 10 bottles of Artichoke Leaf extract because the product is misbranded, an unapproved new drug, and an adulterated dietary 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 the rubric defines as typically resulting in a score of 1 or 2 because it is unlikely to cause adverse health consequences. The specific issues of misbranding and adulteration without reported illness align with a Moderate severity rating.
Plain-English summary
Iowa Select Herbs LLC is recalling 10 bottles of Artichoke Leaf (Cynara Scolymus) extract, 4 fl. Oz. (120 ml), manufactured in Cedar Rapids, IA. The product is identified by Lot 45894 and has an expiration date of 05/2017.
The recall was initiated 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 FDA has classified this recall as Class III, indicating that use of or exposure to the violative product is not likely to cause adverse health consequences.
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, Artichoke Leaf (Cynara Scolymus), 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 - 45894
- 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