Iowa Select Herbs Recalls Juniper Berry Due to Misbranding and Adulteration
Iowa Select Herbs LLC is recalling Juniper Berry products under a consent decree because they are misbranded, unapproved new drugs, and adulterated dietary supplements.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The recall is classified as FDA Class III, which the rubric defines as unlikely to cause adverse health consequences, typically resulting in a Low severity score.
Plain-English summary
Iowa Select Herbs LLC is recalling Juniper Berry (Juniperus communis) products, specifically 1-gallon bottles from Cedar Rapids, Iowa. The recall is being conducted pursuant to a consent decree for injunctive relief. The affected products are identified by Lot 19836 and have an expiration date of 05/2019.
The FDA determined that the recalled products are misbranded, unapproved new drugs, and adulterated dietary supplements. The agency's classification for this recall is Class III.
The recalled product was distributed to retail stores in California, Florida, Georgia, Iowa, Michigan, Missouri, Montana, New York, and South Carolina. It was also distributed to consumers nationwide and internationally in Denmark, Canada, the UK, Australia, and Serbia. Consumers should stop using the product and contact the recalling firm for instructions.
The recalled product
- Product
- Iowa Select Herbs LLC, Juniper Berry (Juniperus communis), www.iowaselectherbs.com, 1 gallon, Cedar Rapids, IA 52402
- Manufacturer
- Iowa Select Herbs LLC
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 2
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 - 19836
- 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