Hi-Tech Pharmaceuticals recalls slimaglutide weight loss aid due to unapproved drug claims and misbranding. Consumers should check product details and contact the company for guidance.
Unapproved Drug Claims and Misbranded.
Hi-Tech Pharmaceuticals is recalling their slimaglutide weight loss aid product because it contains unapproved drug claims and misbranded labeling. This could lead to consumers being misled about the product's safety and effectiveness.
The product is misbranded and makes unapproved drug claims, meaning it is not approved by the FDA for weight loss. This could lead to consumers believing the product is safe and effective when it is not, potentially causing health risks.
People who purchased the slimaglutide weight loss aid from Hi-Tech Pharmaceuticals are affected. Those using the product for weight loss may be at risk of being misled by unapproved drug claims.
Check for the product name 'Slimaglutide Revolutionary Weight Loss Aid with Glucagon-Like Peptide-1 (GLP-1) Receptor Agonist' and lot number C19El8 with an expiration date of May 30.
Look for the product name and lot number C19El8 with expiration date 05/30 on the packaging.
The recall indicates unapproved drug claims and misbranding, so the product may not be safe as advertised. Consult the manufacturer for guidance.
Check the product details and contact Hi-Tech Pharmaceuticals for further instructions.
The recall states unapproved drug claims and misbranding, but does not specify a risk of serious injury. The danger level is unknown.
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-0593-2025 — Hi-Tech Pharmaceuticals Hi-Tech Pharmaceuticals Hello, I own a Hi-Tech Pharmaceuticals that is covered by recall H-0593-2025 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.
