HIGHFDA FOOD

Hi-Tech Pharmaceuticals L-Glutamine Ultra Pure Powder Recall: 85,950 Units (2025)

Hi-Tech Pharmaceuticals recalled 85,950 units of L-Glutamine Ultra Pure Powder distributed to multiple retailers after FDA enforcement over unapproved drug claims. The product’s labeling asserts drug-like benefits without FDA approval. Consumers should not consume the product and should contact Hi-Tech Pharmaceuticals for refund or replacement by mail to 6015-B Unity Drive, Norcross, GA 30071.

Official notice
Hi-Tech PharmaceuticalsFood & BeveragesLot 059960809 Exp Date 06/28

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA FOOD
Recall date
August 6, 2025
Status
ACTIVE
Severity
2/10

Quick Facts at a Glance

Recall Date
August 6, 2025
Hazard Level
HIGH
Brand
Hi-Tech Pharmaceuticals
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
Nationwide (50 states)
At-Risk Groups
GENERAL

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Food Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Hi-Tech Pharmaceuticals
Product type
L-Glutamine Powder
Model numbers
Lot 059960809 Exp Date 06/28
Sizes
500 g
Sold at
Multiple Retailers
Where affected
Nationwide

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    August 6, 2025

  2. Reported by FDA FOOD

    September 24, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

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

About This Product

L-Glutamine is a dietary supplement used by some to support muscle recovery and energy. This recall concerns product labeling that allegedly makes drug-like claims without FDA approval.

Why This Is Dangerous

The hazard arises from unapproved drug claims on product labeling. This misbranding can mislead consumers about efficacy and safety.

Industry Context

This recall is part of efforts to enforce FDA guidelines on drug claims in dietary supplements.

Practical Guidance

How to identify if yours is affected

  1. Check container label for Lot 059960809 and Exp Date 06/28
  2. Verify packaging states 500 g net weight

Where to find product info

Label, packaging, and UPC on the back of the container

What timeline to expect

Refund or replacement typically processed by mail over 4-6 weeks

If the manufacturer is unresponsive

  • Keep copies of all correspondence with the company
  • File a consumer complaint with FDA if the company is slow to respond
  • Consider seeking legal advice for unresponsive recall issues

How to prevent similar issues

  • Verify dietary supplement claims against FDA warning letters and recall notices
  • Check for FDA-regulated or federal-law-violation tags on packaging
  • Purchase supplements from reputable retailers and verify UPCs and batch codes

Documentation advice

Keep the product, packaging, purchase receipts, and all recall communication for records

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Product Details

Brand: Hi-Tech Pharmaceuticals. Product: L-Glutamine Ultra Pure Powder. Net weight: 500 grams. UPC: 8 11836 02362 6. Model/lot: Lot 059960809 Exp Date 06/28. Quantity recalled: 85,950 units. Distribution: Shipped to AL, AR, AZ, CA, CO, CT, DE, FL, GA, GU, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. Recall date: August 6, 2025. Status: Active.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Shipped to 40+ states and territories
  • Active recall as of 2025-09-24

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
2/ 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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