Kindroot Adaptogems

Kindroot LLC recalled Kindroot Adaptogems in an FDA Class II enforcement action reported as F-0573-2020. Inspection by California Department of Public Health found that product label did not include fish as the source of collagen peptides.

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish allergy.

Reactions can begin within minutes to a few hours after eating the product.

People with a diagnosed fish allergy, especially anyone with a history of anaphylaxis.

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Do not eat the product if you have a fish allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-0573-2020 and keep the packaging, lot code and proof of purchase if you have them.

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

This page is normalized from the openFDA enforcement record F-0573-2020. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.