Yamtun7 recalls Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0
Yamtun7 recalls Poseidon Platinum 3500 capsules (1-count per blister) distributed from July 2019 to September 2020 due to containing undeclared sildenafil and tadalafil without FDA approval.
Stop using this now
Marketed Without An Approved NDA/ANDA: Product found to contain undeclared sildenafil and tadalafil making them unapproved drugs for which the safety and efficacy have not been established and therefore subject to recall.
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What happened, in plain English
Yamtun7 is recalling Poseidon Platinum 3500 capsules because they contain undeclared sildenafil and tadalafil without FDA approval. This makes them unapproved drugs with unverified safety and effectiveness, posing a risk of harm to users. Read more at govinfonow.com/recall/36151-yamtun7-poseidon-platinum-3500-capsules-unapproved-drug-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/36151-yamtun7-poseidon-platinum-3500-capsules-unapproved-drug-recall · Updated October 4, 2026 · FDA enforcement record: FDA #D-0654-2021
Cite this page
“Yamtun7 Poseidon Platinum 3500 Capsules: Unapproved Drug Recall.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36151-yamtun7-poseidon-platinum-3500-capsules-unapproved-drug-recall. Based on FDA recall #D-0654-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0654-2021%22&limit=1).
Why it’s dangerous
The capsules contain undeclared sildenafil (Viagra) and tadalafil (Cialis) without FDA approval. These drugs have not been tested for safety and effectiveness, so they could cause serious health issues like heart problems or allergic reactions.
Who’s affected
Anyone who purchased Poseidon Platinum 3500 capsules between July 1, 2019 and September 28, 2020. People using these capsules for erectile dysfunction or other purposes are at risk due to the unapproved ingredients.
How to tell if you have this one
Check for Poseidon Platinum 3500 capsules in 1-count blister packs with UPC 0 95842 05876 0. They were distributed from July 1, 2019, through September 28, 2020.
- Brand
Yamtun7- Product
Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0- Category
Drug
What to do — step by step
Stop Using Now
Immediately stop taking Poseidon Platinum 3500 capsules as they contain unapproved drugs that could cause serious health risks.
Questions people ask
Are these capsules safe to use?
No, these capsules contain undeclared sildenafil and tadalafil without FDA approval, so they are not safe for use.
What should I do if I have these capsules?
Stop using them immediately and contact the manufacturer for instructions.
When were these capsules distributed?
They were distributed from July 1, 2019, through September 28, 2020.
Contact Yamtun7
We’ve drafted a message you can send Yamtun7 to request your refund or repair — edit it as you like.
Subject: Recall D-0654-2021 — Yamtun7 Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in Hello, I own a Poseidon Platinum 3500 capsule, 1-count per blister card, Distributed by: Poseidon, Made in the USA, UPC 0 95842 05876 0 that is covered by recall D-0654-2021 from Yamtun7. 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-0654-2021 (May 11, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0654-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 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.