🔍 RecallPedia

Blue Face Care Kit; Each kit contains: Blue Lavender Cleansing Milk 1 fl oz bottle Lavender Facial Tonic HydroSoul 1 fl oz bottle Rosehip Treatment Facial Serum - BLUE 0.13 fl oz vial Blue Chamomile Day Moisturizer 0.17 fl oz jar Green Tea Clay 0.1 oz jar evanhealy Hand Made in CA by Plant Divas Inc., San Diego, CA 92064

Class I - Dangerous
Recalled: February 27, 2018 Plant Devas Dairy & Eggs Nationwide

What Should You Do?

  1. Check if you have this product:
    LOT Manuf Date Sell By 7310101 8.1.2017 8.1.2019 7350101 9.1.2017 9.1.2019 7400201 10.2.2017 10.2.2019 7440103 11.1.2017 11.1.2019 7480102 12.1.2017 12.1.2019 8010202 1.2.2018 1.2.2020 8050102 2.1.18- 2.12.18 2.1.2020
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Plant Devas Inc
Reason for Recall:
FDA Office of Colors and Cosmetics sampled product and found virulent and excessive numbers of microorganisms.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Blue Face Care Kit; Each kit contains: Blue Lavender Cleansing Milk 1 fl oz bottle Lavender Facial Tonic HydroSoul 1 fl oz bottle Rosehip Treatment Facial Serum - BLUE 0.13 fl oz vial Blue Chamomile Day Moisturizer 0.17 fl oz jar Green Tea Clay 0.1 oz jar evanhealy Hand Made in CA by Plant Divas Inc., San Diego, CA 92064

Product Codes/Lot Numbers:

LOT Manuf Date Sell By 7310101 8.1.2017 8.1.2019 7350101 9.1.2017 9.1.2019 7400201 10.2.2017 10.2.2019 7440103 11.1.2017 11.1.2019 7480102 12.1.2017 12.1.2019 8010202 1.2.2018 1.2.2020 8050102 2.1.18- 2.12.18 2.1.2020

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0929-2018

Related Recalls