HIGH

Hi-Tech Pharmaceuticals L-Glutamine Powder Recalled Over Drug Claims

Hi-Tech Pharmaceuticals recalled 85,950 units of L-Glutamine Ultra Pure Powder on August 6, 2025. The recall follows concerns over unapproved drug claims associated with the product. Consumers should stop using the product and seek a refund or replacement.

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

Product Details

The recalled product is Hi-Tech Pharmaceuticals L-Glutamine Ultra Pure Powder, with a UPC of 8 11836 02362 6. The lot number is 059960809 with an expiration date of June 28, 2025. It was distributed across 50 states and territories.

The Hazard

The product claims unapproved drug benefits, which could mislead consumers about its safety and efficacy. This classification falls under Class III, indicating a high risk of harm.

Reported Incidents

No specific incidents of injury or death have been reported at this time. The recall is proactive to prevent potential misuse of the product.

What to Do

Stop using the product immediately. Contact Hi-Tech Pharmaceuticals for refund or replacement information.

Contact Information

For more information, consumers can visit the FDA recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=H-0591-2025.

Key Facts

  • Recall date: August 6, 2025
  • Quantity recalled: 85,950 units
  • Unapproved drug claims identified
  • Distributed in all 50 states and territories

Safety Assessment

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

Product Details

Model Numbers
Lot 059960809 Exp Date 06/28
Affected States
Nationwide
Report Date
September 24, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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