HIGH

Hi-Tech Pharmaceuticals Recalls Slimaglutide Over Misbranding Risk

Hi-Tech Pharmaceuticals recalled 85,950 units of Slimaglutide on August 6, 2025. The recall is due to unapproved drug claims and misbranding. Consumers should stop using the product immediately and seek a refund or replacement.

Hazard Information

Unapproved Drug Claims and Misbranded.

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 Slimaglutide, a dietary supplement containing GLP-1 receptor agonists. It is sold in bottles of 180 tablets. The affected lot is Lot C19El8 with an expiration date of May 30.

The Hazard

The product contains unapproved drug claims and is considered misbranded. This classification is classified as Class III, indicating a high risk to consumers.

Reported Incidents

No specific incidents of injury or illness related to the product have been reported. The recall is precautionary due to misbranding.

What to Do

Consumers should not consume Slimaglutide. Contact Hi-Tech Pharmaceuticals Inc. for refund or replacement information.

Contact Information

For more details, consumers can visit the FDA's recall page at https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=H-0593-2025.

Key Facts

  • 85,950 units recalled
  • Lot C19El8, Exp Date 05/30
  • Sold across 50 states
  • High hazard due to misbranding
  • Immediate stop-use recommended
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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot C19El8 Exp Date 05/30
Affected States
Nationwide
Report Date
September 24, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE
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