Saini Trade recalls MALEXTRA dietary supplements due to undeclared sildenafil and propoxyphenylsildenafil found in lab tests. Consumers should stop using affected lots.
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Saini Trade is recalling MALEXTRA dietary supplements because lab tests found undeclared sildenafil and propoxyphenylsildenafil. This poses a risk of serious health effects due to unapproved drug ingredients.
The product contains undeclared sildenafil and propoxyphenylsildenafil, which are prescription drugs not approved for dietary supplements. These substances can cause serious health issues like heart problems or unexpected side effects when taken without medical supervision.
Anyone who purchased MALEXTRA dietary supplements with the lot number KT-1ST-43-01-04/2026 (expiring April 2026) from Health Fixer in Tempe, AZ. People using these supplements for health purposes are at risk.
Check the product label for the lot number KT-1ST-43-01-04/2026, which expires April 2026. The product was distributed by Health Fixer in Tempe, AZ, and sold with UPC B0CWKZ6ZP3.
Immediately stop using MALEXTRA dietary supplements with the lot number KT-1ST-43-01-04/2026 as they contain unapproved drugs.
The product contains undeclared sildenafil and propoxyphenylsildenafil, which are prescription drugs not approved for dietary supplements and can cause serious health issues.
Check the product label for the lot number KT-1ST-43-01-04/2026, which expires April 2026. The product was distributed by Health Fixer in Tempe, AZ, and sold with UPC B0CWKZ6ZP3.
Immediately stop using it and contact Saini Trade for further instructions.
We’ve drafted a message you can send Saini Trade to request your refund or repair — edit it as you like.
Subject: Recall D-0464-2025 — Saini Trade Saini Trade Hello, I own a Saini Trade that is covered by recall D-0464-2025 from Saini Trade. 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.
