Iowa Select Herbs Recalls Bitter Melon Supplement Due to Misbranding
Iowa Select Herbs LLC is recalling Bitter Melon 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 is defined as unlikely to cause adverse health consequences. The issues are regulatory (misbranding, unapproved new drug status, adulteration) rather than an acute physical hazard like a pathogen or choking risk.
Plain-English summary
Iowa Select Herbs LLC is recalling Bitter Melon (Momordica charantia) dietary supplements, 32 fl. oz. bottles, manufactured in Cedar Rapids, IA. The recall is being conducted pursuant to a consent decree for injunctive relief, which ordered the firm to recall all products.
The agency determined that the recalled products are misbranded, unapproved new drugs, and adulterated dietary supplements. The specific lot number is 58545F, 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 further instructions.
The recalled product
- Product
- Iowa Select Herbs LLC, Bitter Melon (Momordica charantia, www.iowaselectherbs.com, 32 fl. Oz., Cedar Rapids, IA 52402
- Manufacturer
- Iowa Select Herbs LLC
- Category
- Food — Dietary Supplement
- Affected units
- 1
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 - 58545F
- 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.
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