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Stop using now Drug recall · FDA · Published November 29, 2023

Meta Herbal Magnum XXL 9800: Unapproved Sildenafil Risk

Meta Herbal's Magnum XXL 9800 capsules contain undeclared sildenafil, a prescription drug. Consumers should stop using these products due to unapproved marketing.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0206-2024DrugMeta Herbal ›
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Contact the company

Recalling firmMeta Herbal33 Cordwood Ln · East Hampton, NY 11937-5201
✎ GovInfoNow plain-language explainer

Meta Herbal is recalling Magnum XXL 9800 capsules because they contain sildenafil without proper FDA approval. This poses a risk of serious health issues since sildenafil is a prescription medication. Read more at govinfonow.com/recall/32934-meta-herbal-magnum-xxl-9800-unapproved-sildenafil-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/32934-meta-herbal-magnum-xxl-9800-unapproved-sildenafil-risk · Updated August 17, 2026 · FDA enforcement record: FDA #D-0206-2024

Cite this page

“Meta Herbal Magnum XXL 9800: Unapproved Sildenafil Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32934-meta-herbal-magnum-xxl-9800-unapproved-sildenafil-risk. Based on FDA recall #D-0206-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0206-2024%22&limit=1).

The FDA announced on November 29, 2023, that Meta Herbal is recalling Magnum XXL 9800 capsules because they contain undeclared sildenafil. The agency classified the recall as Class I.

How to tell if you have it

  • Brand: Meta Herbal
  • Product: Magnum XXL 9800, 2000 mg per capsule, 1 capsule per blister pack
  • Distributor: Magnum Los Angelas CA
  • UPC: 6 45759 99300 7
  • Amazon ASINs: B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ
  • Lot codes: All Lots
  • Quantity: 500 blister packs

The hazard

The product was marketed without an approved New Drug Application or Abbreviated New Drug Application. Magnum XXL was found to contain the undeclared active pharmaceutical ingredient sildenafil.

Context

GovInfoNow's records show other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15) and Buy-Herbal Kian Pee Wan Capsules Recall (2026-03-21). SILINTAN 25-pill bottle was also recalled for undeclared meloxicam in an FDA analysis on 2025-10-20.

How to tell if you have this one

Check for Magnum XXL 9800 capsules with 2000 mg per capsule, 1 per blister pack. The UPC is 645759993007. These were sold on Amazon with ASINs B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ.

  • Brand
    Meta Herbal
  • Product
    Magnum XXL 9800, 2000 mg per capsule, 1 capsule per blister pack, Distributed by Magnum Los Angelas CA. UPC 6 45759
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using Magnum XXL 9800 capsules as they contain unapproved sildenafil which can cause serious health risks.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the USA. Product was sold via Amazon's Marketplace.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 35 days after the firm started it.

1. Firm started the recall: Nov 29, 202312. FDA classified it Class I: Dec 27, 202323. Published in FDA’s Enforcement Report: Jan 3, 2024320232024
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Keep exploring

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-0206-2024 (November 29, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0206-2024 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA