Recall Radar

Kindroot recalls kindroot adaptogems: label issue

February 5, 2020 · Kindroot Class II

Class IIFDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.
Reason for the recallInspection by California Department of Public Health found that product label did not include fish as the source of collagen peptides.

Find the official FDA enforcement report

Recall at a glance

Recalling company
Kindroot
Location
Redondo Beach, CA
Reported by FDA
February 5, 2020
Recall started
January 15, 2020
Risk class
Class II
Status (latest data we have)
Terminated
Type
Voluntary: Firm initiated
Category
Supplements and infant formula
Reason type
Labeling and quality

Is my product affected?

Compare your product’s name, size and lot or date codes with the list below. A recall usually covers only specific codes.

  • 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
    Quantity: 39 bags
    Codes: LOT 1109192 LOT 1117192 LOT 1124192 LOT 1221192

Where it was distributed

CA NY, VA and 18 online sales on to customers in CA, OH, AK, CO.

What to do

If you have this product, check the codes above. FDA recall notices often tell consumers to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information, and if you are unsure, do not eat it. If someone becomes ill after eating a recalled food, contact a healthcare professional. See FDA’s recalls and safety alerts for company announcements.

Frequently asked questions

What was recalled?

Kindroot recalled 1 product, including kindroot adaptogems; Peach Blossom Plant lozenges for lit looks. 20 lozenges net wt. 2.6 oz. 74 g - Dietary Supplement UPC: 8 60000 30544….

Why was it recalled?

Inspection by California Department of Public Health found that product label did not include fish as the source of collagen peptides.

What does Class II mean?

FDA’s middle class: use of the product may cause temporary or medically reversible adverse health consequences, or the chance of serious harm is remote.

Where was it sold or shipped?

CA NY, VA and 18 online sales on to customers in CA, OH, AK, CO.

What should I do if I have this product?

Compare the product name, size and lot or date codes with the details on this page. FDA recall notices often tell you to stop eating the product and to return it or throw it away. Follow the company’s instructions and the official FDA information. If you are unsure, do not eat it.

Similar recalls in supplements and infant formula

Sources

Data provided by the U.S. Food and Drug Administration (FDA) through openFDA, shown as published and not validated by this site. This site is independent and is not affiliated with or endorsed by FDA. It covers FDA-regulated foods; meat, poultry and egg products are regulated by USDA. Do not rely on this site for medical decisions: for health concerns contact a healthcare professional, and always follow the official notice and the company’s instructions. Terms and disclaimer.