A New Life Herbs recalls Chaga Mushroom Herbal Supplement due to unapproved drug claims and missing Supplement Facts label. Consumers should check product labels for UPC 284588087831.
Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
A New Life Herbs is recalling its Chaga Mushroom Herbal Supplement because the product makes unapproved health claims and lacks a required Supplement Facts label. This could mislead consumers about the product's effects and safety.
The product makes health claims that are not approved by the FDA, such as 'supports a healthy immune system with anti-cancer' properties. It also lacks a required Supplement Facts label, which is needed for accurate ingredient information.
Anyone who purchased this herbal supplement from retailers. People using it for health purposes may be at risk of being misled by unverified claims.
Check for the product name 'Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract' on a 2 oz. glass dropper bottle. Look for UPC 284588087831 or expiration dates listed on the label.
Look for the UPC code 284588087831 on the bottle to confirm if it's the recalled product.
The product makes unapproved health claims and lacks a required Supplement Facts label, but it does not pose a direct safety risk like injury or illness. The FDA considers it misbranded but not dangerous in normal use.
Check for the UPC 284588087831 on the 2 oz. glass dropper bottle labeled 'Chaga Mushroom Herbal Supplement, 1:5 Alcohol Double Extract'.
The recall does not require immediate action, but you can check the label for the UPC code to confirm if it's affected.
We’ve drafted a message you can send A New Life Herbs to request your refund or repair — edit it as you like.
Subject: Recall H-0344-2026 — A New Life Herbs A New Life Herbs Hello, I own a A New Life Herbs that is covered by recall H-0344-2026 from A New Life Herbs. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
