SELECT DISTRIBUTIONS LLC recalls Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by:
FDA recalls Aphrodisiac Platinum 40000 due to contamination with sildenafil. This unapproved product poses health risks and should not be used.
Recall notice
Marketed without an approved NDA/ANDA: FDA analysis has found the product to be tainted with sildenafil
Contact the company & request your remedy
What happened, in plain English
The FDA has recalled Aphrodisiac Platinum 40000 because it contains sildenafil without proper FDA approval. Using this product could lead to health risks due to the unapproved ingredients. Read more at govinfonow.com/recall/38944-aphrodisiac-platinum-40000-recall-fda-finds-sildenafil-taint-in-unapproved.
Source Summary by GovInfoNow · govinfonow.com/recall/38944-aphrodisiac-platinum-40000-recall-fda-finds-sildenafil-taint-in-unapproved · Updated October 5, 2026 · FDA enforcement record: FDA #D-1344-2019
Cite this page
“Aphrodisiac Platinum 40000 Recall: FDA Finds Sildenafil Taint in Unapproved Product.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38944-aphrodisiac-platinum-40000-recall-fda-finds-sildenafil-taint-in-unapproved. Based on FDA recall #D-1344-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1344-2019%22&limit=1).
Why it’s dangerous
The product was marketed without FDA approval and contains sildenafil, a drug that can cause serious health issues when used without proper oversight. This unapproved product may lead to adverse effects due to the presence of sildenafil.
Who’s affected
Anyone who purchased Aphrodisiac Platinum 40000 from any distributor. People using this product for sexual health purposes are at risk.
How to tell if you have this one
Check for the product name 'Aphrodisiac Platinum 40000' with 24 blister cards per box. The UPC code is 644118128135. All lots are affected.
- Brand
Aphrodisiac- Product
Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by:- Category
Drug
What to do — step by step
Stop Using It Now
Immediately stop using Aphrodisiac Platinum 40000 as it contains sildenafil without FDA approval.
Questions people ask
Is this product safe to use?
No, the product contains sildenafil without FDA approval and poses health risks.
How can I check if I have the recalled product?
Look for the product name 'Aphrodisiac Platinum 40000' with 24 blister cards per box and UPC code 644118128135.
What should I do if I have this product?
Stop using it immediately and contact the manufacturer for further instructions.
Contact Aphrodisiac
We’ve drafted a message you can send Aphrodisiac to request your refund or repair — edit it as you like.
Subject: Recall D-1344-2019 — Aphrodisiac Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 Hello, I own a Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by: that is covered by recall D-1344-2019 from Aphrodisiac. 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-1344-2019 (April 9, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1344-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.