HIGHFDA FOOD

Hi-Tech Pharmaceuticals Slimaglutide 85,950-Unit Recall for Unapproved Drug Claims (2025)

Hi-Tech Pharmaceuticals recalled 85,950 units of Slimaglutide weight loss supplement distributed to more than 40 states. The recall cites unapproved drug claims and misbranding. Consumers who purchased Slimaglutide should not use it and should contact Hi-Tech Pharmaceuticals for refund or replacement per the recall notice.

Official notice

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
7/10

Quick Facts at a Glance

Recall Date
August 6, 2025
Hazard Level
HIGH
Brand
Hi-Tech Pharmaceuticals
Category
Health & Personal Care
Sold At
Unknown
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
Weight loss dietary supplement tablets
Model numbers
Lot C19El8 Exp Date 05/30
Sold at
Unknown
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 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

About This Product

Slimaglutide is marketed as a weight loss aid by Hi-Tech Pharmaceuticals. It is presented as a GLP-1 receptor agonist with added secretagogues, sold as a dietary supplement.

Why This Is Dangerous

The recall cites unapproved drug claims and misbranding. This means the product labeling and marketing did not meet regulatory requirements and could mislead consumers about its effectiveness and safety.

Industry Context

This recall is not described as part of a broader industry pattern in the provided data.

Real-World Impact

Consumers may be exposed to unapproved products and mislabeled health claims. The primary safety concern is regulatory noncompliance rather than injuries reported to date.

Practical Guidance

How to identify if yours is affected

  1. Identify Slimaglutide on packaging
  2. Check Lot C19El8 and Exp 05/30
  3. Verify the product type as a dietary supplement marketed for weight loss

Where to find product info

Labeling on bottle and packaging; FDA recall page H-0593-2025

What timeline to expect

Refunds or replacements typically take 4-8 weeks after proof of claim

If the manufacturer is unresponsive

  • Document all communications with the company
  • File a consumer complaint with CPSC if unresponsive
  • Seek legal advice if you suspect injury or fraud

How to prevent similar issues

  • Avoid dietary supplements with grandiose weight loss claims
  • Look for third-party certifications (USP, NSF)
  • Check FDA recall and FDA warning letters before purchase
  • Prefer brands with transparent labeling and regulatory compliance

Documentation advice

Keep recall letter, purchase receipts, bottle label photos, lot and expiration details, and any correspondence with the company

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Product Details

Brand: Hi-Tech Pharmaceuticals Product: Slimaglutide weight loss supplement Model numbers: Lot C19El8 Exp.Date: 05/30 Quantity recalled: 85,950 units Where sold/shipped: 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: 2025-08-06 Status: ACTIVE Price: Unknown

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • Lot C19El8 Exp 05/30
  • Distributed to states including 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
  • Hazard: Unapproved drug claims and misbranding; No injuries reported

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
7/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeWeight loss dietary supplement tablets
Sold At
Unknown

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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