Meta Herbal's Magnum XXL 9800 capsules contain undeclared sildenafil, a prescription drug. Consumers should stop using these products due to unapproved marketing.
Marketed without an approved NDA/ANDA: Magnum XXL found to contain undeclared active pharmaceutical ingredient (API) - Sildenafil.
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.
The capsules contain sildenafil, a prescription drug for erectile dysfunction, but were marketed without FDA approval. This means they could cause serious health issues like heart problems or strokes if taken without medical supervision.
Anyone who purchased Magnum XXL 9800 capsules from Amazon or other retailers. People using these capsules for erectile dysfunction or other purposes are at highest risk.
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.
Immediately stop using Magnum XXL 9800 capsules as they contain unapproved sildenafil which can cause serious health risks.
Sildenafil is a prescription drug for erectile dysfunction that can cause serious health issues like heart problems if taken without medical supervision.
Check for Magnum XXL 9800 capsules with 2000 mg per capsule, 1 per blister pack. The UPC is 645759993007, and they were sold on Amazon with specific ASINs.
Immediately stop using the capsules and contact Meta Herbal for further instructions.
We’ve drafted a message you can send Meta Herbal to request your refund or repair — edit it as you like.
Subject: Recall D-0206-2024 — Meta Herbal Meta Herbal Hello, I own a Meta Herbal that is covered by recall D-0206-2024 from Meta Herbal. 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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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.
