MS Bionic recalls MegaJex Herbal Supplement, Maximum Formula for Men, Fast acting, Increase Stamina, 20 capsules, MS Bionics, Gardena, CA
MS Bionic recalls MegaJex Herbal Supplement containing sildenafil and tadalafil without FDA approval. These ingredients are in prescription ED drugs. Consumers should check if they have the product with expiration date 12/2019.
Recall notice
Marketed without an Approved NDA/ANDA; product contains sildenafil and tadalafil which are active pharmaceutical ingredients in FDA approved drugs used to treat erectile dysfunction (ED)
Contact the company & request your remedy
What happened, in plain English
MS Bionic is recalling MegaJex Herbal Supplements that contain sildenafil and tadalafil—active ingredients in FDA-approved erectile dysfunction medications. These products were marketed without proper FDA approval, posing risks of serious health effects. Read more at govinfonow.com/recall/42144-ms-bionic-megajex-herbal-supplement-fda-unapproved-sildenafil-tadalafil-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/42144-ms-bionic-megajex-herbal-supplement-fda-unapproved-sildenafil-tadalafil-risk · Updated October 8, 2026 · FDA enforcement record: FDA #D-0472-2017
Cite this page
“MS Bionic MegaJex Herbal Supplement: FDA Unapproved Sildenafil/Tadalafil Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/42144-ms-bionic-megajex-herbal-supplement-fda-unapproved-sildenafil-tadalafil-risk. Based on FDA recall #D-0472-2017 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0472-2017%22&limit=1).
Why it’s dangerous
The product contains sildenafil and tadalafil, which are active pharmaceutical ingredients in FDA-approved drugs for erectile dysfunction. These ingredients were marketed without FDA approval, meaning they could cause serious health issues if used without medical supervision.
Who’s affected
People who purchased MegaJex Herbal Supplements labeled 'Maximum Formula for Men' with expiration date 12/2:2019 are affected. Men using these products for erectile dysfunction treatment are at higher risk due to unapproved ingredients.
How to tell if you have this one
Check for the product name 'MegaJex Herbal Supplement, Maximum Formula for Men' with 20 capsules and expiration date 12/2019. The product was sold by MS Bionic in Gardena, California.
- Brand
MS Bionic- Category
Drug
What to do — step by step
Check Product Details
Look for the product name 'MegaJex Herbal Supplement, Maximum Formula for Men' with 20 capsules and expiration date 12/2019.
Questions people ask
Why is this product being recalled?
The product contains sildenafil and tadalafil, which are active pharmaceutical ingredients in FDA-approved drugs for erectile dysfunction, but was marketed without FDA approval.
What should I do if I have this product?
The recall record does not specify a remedy, so check the product details and contact MS Bionic for further instructions.
Is this product safe to use?
The product was marketed without FDA approval, so it may pose serious health risks and is not considered safe for use without medical supervision.
Contact MS Bionic
We’ve drafted a message you can send MS Bionic to request your refund or repair — edit it as you like.
Subject: Recall D-0472-2017 — MS Bionic MS Bionic Hello, I own a MS Bionic that is covered by recall D-0472-2017 from MS Bionic. 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-0472-2017 (November 30, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0472-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.