A New Life Herbs recalls herbal supplements over unapproved drug claims and missing Supplement Facts labels
The labels on these ginger, chaga, sinus and anti-virus herbal products make drug claims that have not been approved, and the products have no Supplement Facts label, so they are misbranded.
What to do
The notice does not give instructions. Read the official notice for details.
Recall details
- Product
- Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 capsules/560 mg, packaged in a plastic bag; 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; Sinus Cap Herbal Supplement, Herbs containing…
- Company
- A New Life Herbs, LLC
- Hazard
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Units
- 48 bags; 144 bottles; 38 bags
- Where sold
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- FDA classification
- Class II · Terminated
- Classified by FDA
- December 23, 2025
- Recall started
- November 20, 2025
- FDA enforcement report
- December 31, 2025
- Recall closed
- August 28, 2026
- Identifiers
- Codes: C132GR EXP 7/27 C131GR EXP 6/27 C121GR EXP 2/27 C115GR EXP 12/26 C108GR EXP 1/26 C93GR EXP 7/25
- FDA recall number: H-0346-2026
- Codes: T720CH EXP 3/30 T656CH EXP 10/29 T618CH EXP 7/29 T568CH EXP 1/29 T532CH EXP 10/28
- FDA recall number: H-0344-2026
- Codes: C136SC EXP 10/27 C128SC EXP 5/27 C110SC EXP 9/26 C109SC EXP 4/26 C102SC EXP 10/25
- FDA recall number: H-0348-2026
- Codes: T801AV EXP 9/30 T686AV EXP 12/29 T636AV EXP 9/29 T564AV EXP 9/28
- FDA recall number: H-0340-2026
- Codes: T553MF EXP 12/28
- FDA recall number: H-0345-2026
- Codes: E170PA EXP 7/28 E174PA EXP 9/28 E161PA EXP 12/27 E146PA EXP 12/26 E123PA EXP 7/26 E110PA EXP 10/25 E93PA EXP 2/25
- FDA recall number: H-0347-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- Product
- Organic Ginger Root Herbal Supplement, Natural anti-inflammatory properties, supports gut, increases circulation, 50 capsules/560 mg, packaged in a plastic bag | 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 | Sinus Cap Herbal Supplement, Herbs containing antibiotic, drying, expectorant, and emollient properties, Fenugreek, Thyme, Oregon Grape Root, & Bentonite Clay, 50 capsules/510 mg; packaged in a plastic bag | Anti-virus Herbal Supplement, 1:5 Alcohol Tincture, Helps to stop viral replication, expectorant properties, Contains: Forsethia blossoms, Sumac berries, Pine needles; packaged in a 2 oz. glass dropper bottle, UPC 283162814429
- Reason for recall
- Unapproved drug claims on product labeling and product misbranded due to no Supplement Facts label
- Classification
- Class II (Terminated)
- Distribution
- AL, AZ, CA, GA, IL, IN, MN, MO, MS, NC, NY, TN
- Quantity
- 48 bags; 144 bottles; 38 bags; 116 bottles; 22 bottles; 275 bottles
Related recalls
Vitality Works recalls 365 Whole Foods Market Ashwagandha Capsules over possible Salmonella contamination
One lot of the 120 count capsules could be contaminated with Salmonella, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
Primal Supplements Group recalls Primal Herbs Volume herbal supplement because it contains sildenafil not on the label
FDA laboratory analysis confirmed that Primal Herbs Volume contains sildenafil, which is not listed on the product label.
Evexias Health Solutions recalls Amino Ultra capsules because label fails to list fish oil
The Amino Ultra 90-capsule dietary supplement is mislabeled because its label does not declare that it contains fish oil.
Evexias Health Solution · 30 bottles
Tonight We Ride recalls Ultimate Forza Male Supplement capsules over undeclared sildenafil, tadalafil and dapoxetine
The capsules contain sildenafil, tadalafil and dapoxetine that are not listed on the label, which may interact with nitrates and lower blood pressure to dangerous levels.
A&P Creations recalls X10 Natural Enhancement Supplement and biQ-FEL over undeclared Sildenafil and Tadalafil
The notice says X10 Natural Enhancement Supplement and biQ-FEL contain Sildenafil and Tadalafil that are not declared, and it covers 1,283 retail units and 3,116 bottles sold nationwide.
A&p Creations · 4,399 units
Pacific Health Sciences recalls Babies' Magic Tea Baby Sleep Gripe Water over undeclared alcohols
FDA testing of one lot found ethanol, methanol and isopropanol that are not listed on the label, which may pose a risk depending on the amount consumed and the age and body weight of the person using it.
Pacific Health Sciences Llc · 953 units