Hi-Tech Pharmaceuticals recalls their Flexible Joint Formula with Cissus Quadrangulalis for unapproved drug claims. Consumers should check product details and contact the company for guidance.
Unapproved Drug Claims.
Hi-Tech Pharmaceuticals is recalling their Flexible Joint Formula with Cissus Quadrangulalis because it contains unapproved drug claims. This means the product may not be safe for use as advertised.
The product makes unapproved drug claims, which means it could be unsafe or misleading for health purposes. This is a regulatory issue rather than a physical hazard like fire or injury.
People who purchased this supplement for joint health support are likely affected. Those with pre-existing conditions or using the product for medical purposes may be at higher risk.
Check for the product name 'Flexible Joint Formula with Cissus Quadrangulalis' and the UPC 7 97573 90884 1 6015-B. The lot number 405310805 and expiration date 07/28 are also on the label.
Look for the product name, UPC, lot number, and expiration date on the label.
The recall is due to unapproved drug claims, not a physical hazard. The product may not be safe as advertised.
Check for the product name 'Flexible Joint Formula with Cissus Quadrangulalis' and the UPC 7 97573 90884 1 6015-B on the label.
The recall does not specify a remedy, so contact Hi-Tech Pharmaceuticals 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-0586-2025 — Hi-Tech Pharmaceuticals Hi-Tech Pharmaceuticals Hello, I own a Hi-Tech Pharmaceuticals that is covered by recall H-0586-2025 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.