Iowa Select Herbs Recalls Soursop Leaf Product for Misbranding
Iowa Select Herbs LLC is recalling Graviola Leaf "Soursop" 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 recall is classified as FDA Class III, which is defined as unlikely to cause adverse health consequences, aligning with the Moderate severity level for minor labeling or regulatory issues.
Plain-English summary
Iowa Select Herbs LLC is recalling Graviola Leaf "Soursop" (Annona muricata) in 4 fl. Oz. and 16 fl. Oz. bottles. The recall is being conducted 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 specific lot number is 22363, with an expiration date of 09/2020.
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. Consumers should stop using the product and contact the manufacturer for instructions.
The recalled product
- Product
- Iowa Select Herbs LLC, Graviola Leaf "Soursop" (Annona muricata), www.iowaselectherbs.com, (a) 4 fl. Oz., (b) 16 fl. Oz., Cedar Rapids, IA 52402
- Manufacturer
- Iowa Select Herbs LLC
- Category
- Food — Dietary Supplement
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 - 22363
- Expires - 09/2020
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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