Garden of Life Mushroom Supplement Recalled for Undeclared Soy
Garden of Life RM-10 mushroom supplement recalled due to undeclared soy, a common allergen. The recall affects 15,119 bottles distributed domestically and internationally; consumers with soy allergies should not use these products.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA Class II recall for undeclared soy, a common allergen. The source text does not report any illnesses or injuries, and per the severity rubric, allergen mislabeling on common allergens warrants a High rating.
Plain-English summary
Garden of Life, RM-10, Organically Grown Mushrooms dietary supplement is being recalled because the product contains undeclared soy. This poses a risk to consumers with soy allergies or sensitivities.
The recalled product is packaged as 60 vegetarian caplets per bottle. Affected lot numbers are 50298707, 50315317, 50298646, and 50283628, with expiration dates from January 2024 through August 2024. Approximately 15,119 bottles were distributed domestically and internationally.
Consumers who purchased this product should check the lot number and expiration date on their bottle against the recalled batches. Anyone with a soy allergy or sensitivity should stop using the product immediately.
The recalled product
- Product
- Garden of Life, RM-10, Organically Grown Mushrooms, 60 Vegetarian Caplets, Whole Food Dietary Supplement
- Manufacturer
- Garden Of Life Llc
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 15,119
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 (4)
- Lot Numbers: 50298707
- 50315317
- 50298646
- 50283628 Exp. Dates: 1/2024-8/2024
Distribution
Distribution scope not specified by the agency.
Part of a larger recall action
This product is one of 3 recalled by Garden Of Life 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.
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