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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Low RiskFDA Food
Medications & Supplements/Dietary Supplements

Hi-Tech Pharmaceuticals Dietary Supplements Recalled for Unapproved Drug Claims

Agency Publication Date: September 12, 2025
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Summary

Hi-Tech Pharmaceuticals Inc. is voluntarily recalling 85,950 units total of various dietary supplements because they were marketed with unapproved drug claims and are considered misbranded. These products, which include brands like Formutech Nutrition, iForce Nutrition, and Prime Nutrition, were distributed across 48 U.S. states and several territories. Consumers who have these products should stop using them and return them to the store where they were purchased for a full refund.

Risk

These products are being sold with medical claims that have not been evaluated or approved by the FDA, meaning their safety and effectiveness for treating specific health conditions are unknown. Misbranding occurs when a product's labeling is false, misleading, or fails to meet legal requirements, potentially leading consumers to use these items instead of seeking proven medical treatments.

What You Should Do

  1. The recalled products include various dietary supplements under the Hi-Tech Pharmaceuticals, Formutech Nutrition, iForce Nutrition, LG Sciences, Prime Nutrition, and Top Secret Nutrition brands.
  2. Check your supplement containers for specific lot numbers and expiration dates, such as Lot 405310805 (Exp 07/28), Lot 303120691 (Exp 05/28), or Lot C19El8 (Exp 05/30). See the Affected Products section below for the full list of affected codes.
  3. Return the product to the place of purchase for a full refund, throw it away, or contact Hi-Tech Pharmaceuticals Inc. for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) for additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Formutech Nutrition Flexible Joint Formula with Cissus Quadrangularis (240 Capsules)
Variants: 240 Capsules
UPC Codes:
797573908841
Lot Numbers:
405310805 (Exp Date 07/28)
GTIN:
797573908841

Recall #: H-0586-2025

Product: Hi-Tech Pharmaceuticals Adderex XR (30 Tablets)
Variants: 30 Tablets
UPC Codes:
811836026917
Lot Numbers:
303120691 (Exp Date 05/28)
GTIN:
811836026917

Recall #: H-0587-2025

Product: Hi-Tech Pharmaceuticals Beta Sitosterol (90 Tablets)
Variants: 90 Tablets, 715mg
UPC Codes:
811836025873
Lot Numbers:
C1847 (Exp Date 05/29)
GTIN:
811836025873

Recall #: H-0588-2025

Product: Hi-Tech Pharmaceuticals Fish Oil Heart and Brain Health (90 Soft Gels)
Variants: 90 Soft Gels
UPC Codes:
811836025859
Lot Numbers:
517120551 (Exp Date 04/30)
GTIN:
811836025859

Recall #: H-0589-2025

Product: Hi-Tech Pharmaceuticals Joint-RX Dietary Supplement (90CT)
Variants: 90CT
UPC Codes:
857084000354
Lot Numbers:
503110607 (Exp Date 04/30)
GTIN:
857084000354

Recall #: H-0590-2025

Product: Hi-Tech Pharmaceuticals L-Glutamine Ultra Pure Powder (500 Grams)
Variants: 500 Grams, Powder
UPC Codes:
811836023626
Lot Numbers:
059960809 (Exp Date 06/28)
GTIN:
811836023626

Recall #: H-0591-2025

Product: Hi-Tech Pharmaceuticals Pine Bark Dietary Supplement (60 Tablets)
Variants: 60 Tablets
UPC Codes:
811836024463
Lot Numbers:
C15Cl4 (Exp Date 10/26)
GTIN:
811836024463

Recall #: H-0592-2025

Product: Hi-Tech Pharmaceuticals Slimaglutide Weight Loss Aid (180 Tablets)
Variants: 180 Tablets
Lot Numbers:
C19El8 (Exp Date 05/30)

Recall #: H-0593-2025

Product: Hi-Tech Pharmaceuticals Quercetin (120 Tablets)
Variants: 120 Tablets
UPC Codes:
811836024913
Lot Numbers:
C1612 (Exp Date 08/27)
GTIN:
811836024913

Recall #: H-0594-2025

Product: IFN iForce Nutrition Joint Help (120 Capsules)
Variants: 120 Capsules
UPC Codes:
854503002265
Lot Numbers:
101330812 (Exp Date 01/25)
GTIN:
854503002265

Recall #: H-0595-2025

Product: LG Sciences Battle Hardener Platinum Series
Variants: 6 Week Cycle
UPC Codes:
744890941516
Lot Numbers:
Cl 78216691877 (Exp Date 02/28)
GTIN:
744890941516

Recall #: H-0596-2025

Product: Prime Nutrition Phytoform Fruits & Greens Kiwi-Strawberry (13.75 oz)
Variants: 13.75 oz, Kiwi-Strawberry
UPC Codes:
689466706192
Lot Numbers:
207460659 (Exp Date 10/25)
GTIN:
689466706192

Recall #: H-0597-2025

Product: Prime Nutrition Taurine Dietary Supplement (8.12 oz)
Variants: 8.12 oz, Powder
UPC Codes:
689466706017
Lot Numbers:
710581618 (Exp Date 12/26)
GTIN:
689466706017

Recall #: H-0598-2025

Product: Top Secret Nutrition Extra Strength Uric Control (30 Veggie Caps)
Variants: 30 Veggie Caps
UPC Codes:
811226021584
Lot Numbers:
C1238 (Exp Date 01/25)
GTIN:
811226021584

Recall #: H-0599-2025

Product: Prime Nutrition Phytoform Fruits & Greens Peach Mango (13.75 oz)
Variants: 13.75 oz, Peach Mango
UPC Codes:
638302409063
Lot Numbers:
202140114 (Exp Date 03/27)
GTIN:
638302409063

Recall #: H-0600-2025

Product: Prime Nutrition Phytoform Fruits & Greens Watermelon (13.75 oz)
Variants: 13.75 oz, Watermelon
UPC Codes:
638302409056
Lot Numbers:
174271126 (Exp Date 09/26)
GTIN:
638302409056

Recall #: H-0601-2025

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97373
Status: Resolved
Manufacturer: Hi-Tech Pharmaceuticals Inc.
Sold By: Retailers nationwide; Authorized supplement distributors
Manufactured In: United States
Units Affected: 16 products (85,950 units total)
Distributed To: Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Guam, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Vermont, Washington, Wisconsin, West Virginia, Wyoming

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.