HIGH

Hi-Tech Pharmaceuticals Recalls Joint-RX Supplement Over Drug Claims

Hi-Tech Pharmaceuticals recalled 85,950 units of its Joint-RX dietary supplement on August 6, 2025. The recall occurred due to unapproved drug claims related to the product. Consumers should not consume this supplement and should seek refunds or replacements.

Quick Facts at a Glance

Recall Date
August 6, 2025
Hazard Level
HIGH
Brand
Hi-Tech Pharmaceuticals
Category
Food & Beverages
Sold At
Multiple Retailers
Geographic Scope
Nationwide (50 states)
At-Risk Groups
GENERAL

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

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Product Details

The recalled product is Hi-Tech Pharmaceuticals Joint-RX dietary supplement, 600mc, sold in 90-count bottles. The lot number is 503110607 with an expiration date of April 30. The product shipped to various states including California and Texas.

The Hazard

The product makes unapproved drug claims, which can mislead consumers about its effectiveness. Such claims can pose potential health risks if consumers rely on the product for treatment.

Reported Incidents

No specific injuries or incidents have been reported related to this recall. The FDA classified this recall as Class III, indicating that use of the product is unlikely to cause adverse health consequences.

What to Do

Consumers who purchased this product should not consume it. They should contact Hi-Tech Pharmaceuticals for refund or replacement information.

Contact Information

For refunds or replacements, contact Hi-Tech Pharmaceuticals Inc. at their address: 6015-B Unity Dr, Norcross, GA 30071. Further information is available at their website.

Key Facts

  • Recall date: August 6, 2025
  • Quantity recalled: 85,950 units
  • Sold in multiple states
  • Hazard: Unapproved drug claims
  • Classification: Class III

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Safety Assessment

Risk LevelHIGH
Severity Score
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot 503110607 Exp Date 04/30
Affected States
Nationwide
Report Date
September 24, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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