HIGH

Hi-Tech Pharmaceuticals Recalls Detox Supplement Over Misbranding

Hi-Tech Pharmaceuticals recalled 85,950 units of Phytoform Fruits & Greens Formula on August 6, 2025. The product contains unapproved drug claims and is misbranded. Consumers should not consume the product and seek a refund.

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 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

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Product Details

The recall involves Phytoform Fruits & Greens Formula, 30 servings, sweetened with monk fruit and peach mango flavor. The product weighs 13.75 ounces (390g) and has the UPC 6 38302 40906 3. It was distributed across multiple states.

The Hazard

The product makes unapproved drug claims and is classified as misbranded by the FDA. This can mislead consumers regarding its intended use and effectiveness.

Reported Incidents

No injuries or health incidents have been reported related to this product at this time. The recall is based on labeling and marketing violations.

What to Do

Consumers should stop using the product immediately. Contact Hi-Tech Pharmaceuticals for information on refunds or replacements.

Contact Information

For refunds, consumers can reach Hi-Tech Pharmaceuticals at the provided contact information on the recall notice. Further details are available on the FDA's website.

Key Facts

  • Product sold in 30-serving containers
  • Distributed in 50 states including CA, NY, TX
  • Recall due to unapproved drug claims
  • Consumers advised to not consume the product

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Safety Assessment

Risk LevelHIGH
Severity Score
5/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product Details

Model Numbers
Lot 202140114 Exp Date 03/27
Affected States
Nationwide
Report Date
September 24, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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