Recall record at a glance
| Official record | F-0924-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Plant Devas Inc. |
| Report date | Mar 21, 2018 |
| Recall initiation date | Feb 27, 2018 |
| Quantity | 500 kits |
| Location | Poway, CA, United States |
Official product description
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 Clay) Rhassonl Clay (Moroccan Lava Clay. evanhealy Hand Made in CA by Plant Divas Inc., San Diego, CA 92064
Why the product was recalled
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Distribution information
One distributor in WI. On line sales nationwide and to Argentina, Australia, Austria, Belgium, Bermuda, Canada, China, Costa Rica, Croatia, Czech Republic, Denmark, Dominican Republic, Estonia, Finland, French Polynesia, France, Germany, Greece Hong Kong, India, Indonesia, Ireland, Israel, Italy, Japan, Kuwait, Malaysia. Mexico, Morocco, Netherlands, New Zealand, Nigeria, Norway, Peru, Puerto Rico, Russia, SAR China, Saudi Arabia, Singapore, South Korea, Spain, Sweden, Switzerland, Taiwan, UAE, United Kingdom, Venezuela Distribution also to evanhealy retailers nationwide
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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