Arise & Shine Bentonite Supplement Recalled for Iron Mislabeling
Arise & Shine is recalling Hydrated Bentonite dietary supplements because the label incorrectly states 0% Daily Value of iron, while the product actually contains 106%.
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 II, which typically involves minor labeling errors or low-risk contamination. The hazard is a mislabeling of iron content, which is a nutritional information error rather than a high-risk pathogen or allergen issue.
Plain-English summary
Arise & Shine Herbal Products, Inc. is voluntarily recalling approximately 24,794 32-ounce pouches of Hydrated Bentonite Dietary Supplement Extra Thick Formula. The recall is due to a mislabeling error regarding the iron content of the product.
The product is labeled as containing 0% Daily Value of iron, but it actually contains 106% Daily Value of iron. The affected product is packaged in a foil pouch with a plastic screw-on lid and is distributed worldwide. The recall covers specific lot numbers and expiration dates ranging from 2011 to 2014, with expiration dates extending into 2017.
Consumers who have purchased this product should check their lot numbers against the list provided in the official recall notice. If the product matches the recalled lots, consumers should stop using it and follow the instructions provided by the manufacturer or the FDA for disposal or return.
The recalled product
- Product
- The product is labeled in part "***Arise & Shine Hydrated Bentonite Dietary Supplement Extra Thick Formula 32 FL OZ ***% Daily Value Iron 0***Distributed by: Arise & Shine Herbal Products 562 Parsons Drive Medford, Oregon 97501***" Product is packaged in a foil pouch with a plas
- Manufacturer
- Arise & Shine Herbal Products, Inc.
- Category
- Food — Dietary Supplement
- Hazard
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 (20)
- 2011 LOT/EXP DATE: 3461106 -12/2014
- 3431106 -12/2014
- 3411106 -12/2014
- 3201106 - 11/2014
- 3191106 - 11/2014
- 3141106 - 11/2014
- 2991106 - 11/2014
- 2711106 - 10/2014
- 2571106 - 09/2014
- 2561106 - 09/2014
- 2351106 - 09/2014
- 2221106 - 08/2014
- 2091106 - 07/2014
- 1941106 - 07/2014
- 1801106 - 06/2014. 2012 LOT/EXP DATE: 3541206 - 01/2016
- 3421206 - 12/2015
- 3141206 - 11/2015
- 3131206 - 11/2015
- 3001206 - 11/2015
- 2851206 - 10/2015
Distribution
Distribution scope not specified by the agency.
Related recalls
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