HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH GLUCAGON-LIKE PEPTIDE-1 (GLP-1) RECEPTOR AGONIST
Summary
The FDA issued a Class III for HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH GLUCAGON by Hi-Tech Pharmaceuticals Inc.. Reason: Unapproved Drug Claims and Misbranded..
Details
Source
Food Recall
External ID
H-0593-2025
Action Date
2025-09-24
Status
Terminated
Category
food
Product Description
HI-TECH PHARMACEUTICALS SLIMAGLUTIDE REVOLUTIONARY WEIGHT LOSS AID WITH GLUCAGON-LIKE PEPTIDE-1 (GLP-1) RECEPTOR AGONIST AND SECRETAGOGUES NOVEL GIP (GLUCOSE-DEPENDENT ISNULINOTROPIC POLYPEPTIDE) RECEPTOR AGONIST 180 TABLETS DIETARY SUPPLEMENT
Lot/Code Info: Lot C19El8 Exp Date 05/30
Quantity Affected: 85,950 units total
Reason for Recall
Unapproved Drug Claims and Misbranded.
Distribution
Product was shipped to the following states: 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.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-08-06
Company
Norcross, GA
Context & Analysis
This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.
This was one of 51 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Hi-Tech Pharmaceuticals Inc. has 16 FDA actions in our database, including 16 recalls.
Frequently Asked Questions
What is a Class III recall?
A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Hi-Tech Pharmaceuticals Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Hi-Tech Pharmaceuticals Inc. have FDA actions?
Hi-Tech Pharmaceuticals Inc. has 16 FDA actions in our database, including 16 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0593-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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