FDA recalls Supercore Hard Steel Capsules due to undeclared acetaminophen and sildenafil in products marketed without FDA approval. Consumers should stop using these capsules immediately.
Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Supercore Products Group recalled hard steel capsules sold in blister packs of 10, 20, or 30 units. The capsules were found to contain undeclared acetaminophen and sildenafil, which could pose health risks since they were marketed without FDA approval.
The capsules were marketed without FDA approval and contain undeclared acetaminophen (a painkiller) and sildenafil (a medication for erectile dysfunction). These ingredients could cause serious health issues if taken without proper medical supervision.
Anyone who purchased Supercore Hard Steel Capsules in the U.S. between the manufacturing dates. People using these capsules for pain relief or sexual health purposes are at the highest risk due to the undeclared ingredients.
Check for hard steel capsules in blister packs of 10, 20, or 30 units. The product was manufactured in the U.S.A. and all lots are affected.
Immediately stop using Supercore Hard Steel Capsules as they contain undeclared acetaminophen and sildenafil.
The recall applies to all lots manufactured in the U.S.A. No specific lot numbers are listed.
Stop using them immediately and contact Supercore Products Group for further instructions.
No, the capsules contain undeclared ingredients that could cause serious health risks.
We’ve drafted a message you can send Supercore Products Group to request your refund or repair — edit it as you like.
Subject: Recall D-0003-2025 — Supercore Products Group Supercore Products Group Hello, I own a Supercore Products Group that is covered by recall D-0003-2025 from Supercore Products Group. 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.
