kindroot adaptogems; Peach Blossom Plant lozenges for lit looks. 20 lozenges net wt. 2.6 oz. 74 g - Dietary Supplement UPC: 8 60000 30544 0 Ingredients: Marine collagen Peptides, Ashwagandha Root Extract (organic). Other ingredients: Organic Brown Rice Syrup, malic acid and natural flavor. Unwrap one tablet as needed. Produced by: Kindroot LLC 214 Main Street, El Segundo, CA 90245

Class I - Dangerous
Recalled: January 15, 2020 Kindroot Produce

What Should You Do?

  1. Check if you have this product:
    LOT 1109192 LOT 1117192 LOT 1124192 LOT 1221192
  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:
Kindroot LLC
Reason for Recall:
Inspection by California Department of Public Health found that product label did not include fish as the source of collagen peptides.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

kindroot adaptogems; Peach Blossom Plant lozenges for lit looks. 20 lozenges net wt. 2.6 oz. 74 g - Dietary Supplement UPC: 8 60000 30544 0 Ingredients: Marine collagen Peptides, Ashwagandha Root Extract (organic). Other ingredients: Organic Brown Rice Syrup, malic acid and natural flavor. Unwrap one tablet as needed. Produced by: Kindroot LLC 214 Main Street, El Segundo, CA 90245

Product Codes/Lot Numbers:

LOT 1109192 LOT 1117192 LOT 1124192 LOT 1221192

Distribution:

Distributed in: CA, NY, VA, OH, AK, CO

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-0573-2020

Related Recalls