Today The World recalls Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC,
FDA found undeclared nortadalafil in Today The World's Arize Herbal Dietary Supplement, making it an unapproved drug. Consumers should stop using due to potential health risks.
Stop using this now
Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared nortadalafil, an ingredient found in FDA approved product for the treatment of male sexual enhancement, making this drug an unapproved drug.
Contact the company & request your remedy
What happened, in plain English
Today The World is recalling Arize Herbal Dietary Supplements because they contain undeclared nortadalafil, an ingredient approved for male sexual enhancement. This makes the product an unapproved drug that could pose health risks. Read more at govinfonow.com/recall/32831-arize-herbal-supplement-recall-unapproved-drug-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/32831-arize-herbal-supplement-recall-unapproved-drug-risk · Updated September 23, 2026 · FDA enforcement record: FDA #D-0345-2024
Cite this page
“Arize Herbal Supplement Recall: Unapproved Drug Risk.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/32831-arize-herbal-supplement-recall-unapproved-drug-risk. Based on FDA recall #D-0345-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0345-2024%22&limit=1).
Why it’s dangerous
The product contains undeclared nortadalafil, a substance approved for male sexual enhancement. This makes it an unapproved drug that could cause health issues if taken without proper medical supervision.
Who’s affected
Anyone who owns or uses the Arize Herbal Dietary Supplement (10-capsule boxes) distributed by Natural Herbal Remedies, LLC. People most at risk are those who have taken the supplement without knowing it contains an unapproved drug.
How to tell if you have this one
Check for Arize Herbal Dietary Supplements in 10-capsule boxes with lot number 2107, expiring 10/31/2024. The product was distributed by Natural Herbal Remedies, LLC in Cheyenne, WY.
- Brand
Today The World- Category
Drug
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Ongoing- Distribution
Product distributed nationwide within the United States.
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0343-2024 | Sustain Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by VSD Productions, Inc. Las Vegas, Nevada; Lot #: BTH:230551, Exp. Date 12.05.2026; BTH:230571, Exp. Date 14.05.2026 | 7000 boxes |
| D-0344-2024 | SCHWINNNG Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Today the World LLC, Vancouver, WA 98683; Lot #: 2108, Exp. Date 10/31/2024. | 11500 boxes |
| D-0345-2024 | Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001, www.getarize.com; Lot #: 2107, Exp. Date 10/31/2024. | 5500 boxes |
What to do — step by step
Stop Using Now
Immediately stop using the Arize Herbal Dietary Supplement as it contains an unapproved drug ingredient.
Questions people ask
Is this product safe to take?
No, the product contains undeclared nortadalafil, an unapproved drug ingredient that could pose health risks.
How can I check if I have the recalled product?
Check for Arize Herbal Dietary Supplements in 10-capsule boxes with lot number 2107, expiring 10/31/2024.
What should I do if I have the product?
Immediately stop using it and contact the manufacturer for further instructions.
Contact Today The World
We’ve drafted a message you can send Today The World to request your refund or repair — edit it as you like.
Subject: Recall D-0345-2024 — Today The World Today The World Hello, I own a Today The World that is covered by recall D-0345-2024 from Today The World. 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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Where this comes from
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.
- Official source: FDA Recall #D-0345-2024 (February 6, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0345-2024 to see it in context.
- Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.