Arize Herbal Dietary Supplement — Class I drug recall D-0345-2024
Ongoing recall by Today The World, reported 2024-02-28, distributed nationwide. Marketed Without An Approved NDA/ANDA: FDA analysis found the product to be tainted with undeclared nortadalaf
| Recall number | D-0345-2024 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Today The World, Portland, OR, United States |
| Recall initiated | 2024-02-06 |
| Classified | 2024-02-22 |
| Reported by FDA | 2024-02-28 |
| Distributed | Nationwide (US) |
| Quantity | 5,500 boxes |
| Reason classes | undeclared allergen, unapproved product |
| Lot numbers | 2107 |
| Expiration dates | 2024-10-31 |
Product
Arize Herbal Dietary Supplement, packaged in 10 capsules per box, Distributed by: Natural Herbal Remedies, LLC, Cheyenne, WY 82001, www.getarize.com
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0345-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.