Magnum XXL 9800 — Class I drug recall D-0206-2024
Ongoing recall by Meta Herbal, reported 2024-01-03, distributed nationwide. Marketed without an approved NDA/ANDA: Magnum XXL found to contain undeclared active pharmaceutical ingredient
| Recall number | D-0206-2024 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Meta Herbal, East Hampton, NY, United States |
| Recall initiated | 2023-11-29 |
| Classified | 2023-12-27 |
| Reported by FDA | 2024-01-03 |
| Distributed | Nationwide (US) |
| Quantity | 500 blister |
| Reason classes | undeclared allergen, unapproved product |
| UPC / GTIN / UDI-DI | 00645759993007 |
Product
Magnum XXL 9800, 2000 mg per capsule, 1 capsule per blister pack, Distributed by Magnum Los Angelas CA. UPC 6 45759 99300 7. Amazon's ASIN# B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ
Reason for recall
Marketed without an approved NDA/ANDA: Magnum XXL found to contain undeclared active pharmaceutical ingredient (API) - Sildenafil.
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-0206-2024. 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.