Plant Devas Clay Mask Kit Recalled for Excessive Microorganisms
Plant Devas Inc. is recalling 500 kits of the evanhealy Clay Mask Kit because FDA testing found excessive and virulent microorganisms.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The FDA classified this recall as Class II, and the source text explicitly states that the product contained 'virulent' microorganisms, which meets the criteria for a Severe rating due to the potential for significant health impact.
Plain-English summary
Plant Devas Inc. is recalling 500 kits of the evanhealy Clay Mask Kit. The product includes two glass jars of clay (Green Tea Clay and French Rose Clay), a fan mask brush, and a terra cotta mixing bowl. The kits were distributed to one distributor in Wisconsin, sold online nationwide and internationally, and sold to evanhealy retailers nationwide.
The FDA Office of Colors and Cosmetics sampled the product and found virulent and excessive numbers of microorganisms. The agency has classified this recall as Class II. Specific lot numbers and manufacturing dates are listed in the recall documentation.
Consumers who purchased this product should stop using it immediately. The source text does not specify a refund or replacement process, but consumers should contact the recalling firm or retailer for instructions on how to dispose of or return the product.
The recalled product
- Product
- Clay Mask Kit; 2 glass jars of clay: Green Tea Clay 0.3 oz., and French Rose Clay 0.4 oz. 1 fan mask brush; and 1 terra cotta mixing bowl. Ingredients: Green tea clay, Green (Montmorillonite) clay, Organic Green Tea (Camellia Sinensis) French Rose Clay, Rose Clay (Kaolin Cl
- Manufacturer
- Plant Devas Inc
- Category
- Consumer Product — Cosmetics
- Hazard
- Affected units
- 500
Distribution
Part of a larger recall action
This product is one of 8 recalled by Plant Devas Inc 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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