HIGH

Hi-Tech Pharmaceuticals Recalls Fruits & Greens Supplement Over Misbranding

Hi-Tech Pharmaceuticals recalled 85,950 units of its Phytoform Fruits & Greens Formula on August 6, 2025, due to unapproved drug claims. The product, sweetened with monk fruit and flavored kiwi-strawberry, poses health risks from misleading labeling. Consumers should not consume the product and seek refunds immediately.

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 recalled product is Phytoform Fruits & Greens Formula, 30 servings, net weight 13.75 oz (390g). It has a UPC of 6 89466 70619 2 and the lot number is 207460659 with an expiration date of October 25, 2025.

The Hazard

The product is misbranded and makes unapproved drug claims, which can mislead consumers regarding its safety and efficacy. Misbranding could potentially lead to adverse health effects if consumers rely on false information.

Reported Incidents

There are no specific incidents or injuries reported related to this recall. However, the product's misbranding raises concerns about consumer safety.

What to Do

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

Contact Information

For refunds or replacements, consumers can contact Hi-Tech Pharmaceuticals Inc. directly at their facility in Norcross, GA. More information is available at the FDA's recall notice.

Key Facts

  • 85,950 units recalled
  • Unapproved drug claims
  • Sold in multiple states
  • Contact for refunds
  • Expiration date: 10/25

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Safety Assessment

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

Product Classification

Product TypeDietary Supplement
Sold At
Multiple Retailers

Product Details

Model Numbers
Lot 207460659 Exp Date 10/25
Affected States
Nationwide
Report Date
September 24, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

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