HIGH

Hi-Tech Pharmaceuticals Recalls Joint Supplement Over Unapproved Claims

Hi-Tech Pharmaceuticals recalled 85,950 units of its Flexible Joint Formula on August 6, 2025. The recall follows concerns over unapproved drug claims associated with the product. It was distributed across 50 states and U.S. territories.

Hazard Information

Unapproved Drug Claims.

What You Should Do

Consumers who have purchased this product should not consume it. Contact Hi-Tech Pharmaceuticals Inc. for refund or replacement information. Notification method: Letter

Product Details

The recalled product is Hi-Tech Pharmaceuticals Flexible Joint Formula, which contains 240 capsules per bottle. The specific lot affected is 405310805 with an expiration date of July 28. The product was shipped to various states including California, Florida, and New York.

The Hazard

The recall stems from unapproved drug claims related to the product's ability to support tendons, muscles, and cartilage. This classification falls under Class III, indicating the potential for harm due to misleading claims but not immediate danger.

Reported Incidents

No specific incidents, injuries, or deaths have been reported in relation to this recall. The recall is precautionary due to the product's misleading claims.

What to Do

Consumers should stop using the product immediately. Contact Hi-Tech Pharmaceuticals for refund or replacement information.

Contact Information

Consumers can reach Hi-Tech Pharmaceuticals at their official website or through customer service for more details on the recall.

Key Facts

  • 85,950 units recalled
  • Unapproved drug claims identified
  • Distributed in all 50 states and territories
  • Immediate stop-use recommended
  • Consumers can request refunds or replacements
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Safety Assessment

Risk LevelHIGH
Severity Score
6/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeJoint Health Supplement
Sold At
Multiple Retailers

Product Details

Model Numbers
Lot 405310805 Exp Date 07/28
Affected States
Nationwide
Report Date
September 24, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE
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