Hi-Tech Pharmaceuticals recalls heart health supplements due to unapproved drug claims and misbranding. Consumers should check product labels for UPC 811836024463 and contact the company for details.
Unapproved Drug Claims and Misbranded.
Hi-Tech Pharmaceuticals is recalling heart health supplements that make unapproved drug claims and are misbranded. This means the product could be misleading about health benefits and not meet regulatory standards.
The supplements make health claims that are not approved by the FDA as drugs. They are misbranded because they are marketed as drugs but are actually dietary supplements. This can lead to misleading health information and potential regulatory issues.
People who bought the heart health supplements with UPC 811:836024463 from Hi-Tech Pharmaceuticals in the U.S. are affected. Those most at risk are consumers who rely on these supplements for health benefits.
Check the product label for the UPC 811836024463. The product is a dietary supplement sold by Hi-Tech Pharmaceuticals in the U.S. with a lot number C15Cl4 and expiration date 10/26.
Look for the UPC code 811836024463 on the supplement packaging.
The supplements have unapproved drug claims and are misbranded, meaning they make health claims that are not approved by the FDA as drugs.
Check the product label for the UPC 811836024463. The product was sold by Hi-Tech Pharmaceuticals with a lot number C15Cl4 and expiration date 10/26.
The recall does not specify a remedy, so contact Hi-Tech Pharmaceuticals directly for guidance.
We’ve drafted a message you can send Hi-Tech Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall H-0592-2025 — Hi-Tech Pharmaceuticals Hi-Tech Pharmaceuticals Hello, I own a Hi-Tech Pharmaceuticals that is covered by recall H-0592-2025 from Hi-Tech Pharmaceuticals. 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.
