HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilage & Ease Pain Revolutionary Joint Suppor
Summary
The FDA issued a Class III for HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilag by Hi-Tech Pharmaceuticals Inc.. Reason: Unapproved Drug Claims..
Details
Source
Food Recall
External ID
H-0590-2025
Action Date
2025-09-24
Status
Terminated
Category
food
Product Description
HI-TECH PHARMACEUTICALS JOINT-RX DIETARY SUPPLEMENT 600mc Helps Rebuild Cartilage & Ease Pain Revolutionary Joint Support System 90CT UPC 8 57084 00035 4 Hi-Tech Pharmaceuticals, Inc. 6015-B Unity Dr Norcross, GA 30071
Lot/Code Info: Lot 503110607 Exp Date 04/30
Quantity Affected: 85,950 units total
Reason for Recall
Unapproved Drug Claims.
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-0590-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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