Recall Weekly
Moderate riskFDA FoodClass II

A New Life Herbs Chaga supplement recalled for unapproved drug claims

A New Life Herbs Chaga Mushroom herbal supplement is being recalled because the label makes unapproved health claims (such as anti-cancer properties) and is missing required supplement information. The product does not meet FDA labeling standards for dietary supplements.

From the FDA notice · Read the official notice ↗

What to do

  1. Stop using this product if you have one of the affected batches (lot codes: T720CH, T656CH, T618CH, T568CH, or T532CH)
  2. Do not take any remaining doses
  3. Contact the retailer where you purchased it for a refund or disposal instructions
Official notice ↗

Is yours affected?

Compare your label or packaging with the recalled product.

Product
Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properties; packaged in a 2 oz. glass dropper bottle, UPC 284588087831
UPC code
  • 284588087831
Sold in
AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
Made for
Adults

This recall covers 9 products — see all of them.

Details

Units affected
144 bottles
Illnesses reported
None reported
Manufactured in
17745 Us Highway 64, N/A, Somerville, TN, United States
Classification
Class II
Recall number
H-0344-2026

In the FDA's words

Description
Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract, Supports a healthy immune system with anti-cancer properties; packaged in a 2 oz. glass dropper bottle, UPC 284588087831 Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label T720CH EXP 3/30 T656CH EXP 10/29 T618CH EXP 7/29 T568CH EXP 1/29 T532CH EXP 10/28 Distribution: AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN Affected quantity: 144 bottles
Hazard
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label

9 products in this recall

A New Life Herbs supplements recalled for unapproved drug claims

A New Life Herbs is recalling nine herbal supplement products sold as alcohol tincture, capsule, and dropper-bottle products, including products for immune, pain, sinus, and baby-care use. The FDA says the labels make unapproved drug claims and the products lack a Supplement Facts label. The products were distributed in AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, and TN, and no injuries have been reported.

The agency lists each product separately. Check every one you might have.

Related topics

False claimsUnapproved drugsFoodSupplementsALAZCAGAILINMNMOMSNCNYTNMore from FDA Food