HIGH

Hi-Tech Pharmaceuticals Joint-RX Dietary Supplement Recalled for Unapproved Drug Claims (2025)

Hi-Tech Pharmaceuticals recalled Joint-RX, a 600 mcg dietary supplement sold nationwide, after regulators flagged unapproved drug claims. The recall affects 85,950 units shipped to more than 40 states. Consumers should stop using the product and contact the company for refunds or replacements.

Quick Facts at a Glance

Recall Date
August 6, 2025
Hazard Level
HIGH
Brand
Hi-Tech Pharmaceuticals
Category
Food & Beverages
Sold At
Unknown
Geographic Scope
Nationwide (50 states)
At-Risk Groups
GENERAL

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

Get instant alerts for Food & Beverages recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

About This Product

Joint-RX is a dietary supplement marketed for joint support. Consumers may buy it for perceived cartilage support and pain relief.

Why This Is Dangerous

The hazard stems from unapproved drug claims, meaning the product is marketed with drug-like effects without FDA approval.

Industry Context

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

Real-World Impact

Consumers should stop using Joint-RX and seek refunds or replacements. No injuries reported, but the product should be returned.”

Practical Guidance

How to identify if yours is affected

  1. Check product label for UPC 8 57084 00035 4 and Lot 503110607 Exp 04/30
  2. Verify package shows Joint-RX 600mcg and 90CT
  3. Confirm it's distributed in the states listed

Where to find product info

FDA recall report H-0590-2025 and Hi-Tech Pharmaceuticals recall communications

What timeline to expect

Refunds/Replacements likely processed within 4-8 weeks after submission

If the manufacturer is unresponsive

  • Escalate to consumer protection agencies
  • File a complaint with CPSC/FDA if needed
  • Consult legal counsel for unresponsive company

How to prevent similar issues

  • Buy dietary supplements from reputable brands with verifiable claims
  • Check for FDA warning letters and recall notices before purchase
  • Keep receipts and packaging for recalls
  • Register products where possible for recall alerts

Documentation advice

Save recall letter, photos of product and UPC, and correspondence with Hi-Tech Pharmaceuticals

Product Details

Brand: Hi-Tech Pharmaceuticals. Product: Joint-RX Dietary Supplement 600mcg. Size: 90 count. UPC: 8 57084 00035 4. Lot: 503110607. Expiration: 04/30. Quantity: 85,950 units. Sold/distributed: 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.

Reported Incidents

No injuries or incidents have been reported in connection with this recall.

Key Facts

  • 85,950 total units recalled
  • UPC 8 57084 00035 4
  • Lot 503110607 Exp 04/30
  • Shipped to 40+ states including CA, FL, GA, NY
  • Active recall as of 2025-08-06 with report dated 2025-09-24
View Original Recall on FDA - Food Safety

Browse More Recalls

More from FDA_FOODFood & Beverages

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

Get Alerts for Food & Beverages Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
OTHER

Product Classification

Product TypeDietary Supplement (Joint Support)
Sold At
Unknown

Product Details

Model Numbers
Lot 503110607 Exp Date 04/30
Affected States
Nationwide
Report Date
September 24, 2025
Source Agency
FDA - Food Safety
Recall Status
ACTIVE

Related Recalls

Food & Beverages
HIGH

Prime Nutrition PhytoForm Fruits & Greens Recall 85,950 Units Over Unapproved Drug Claims (2025)

Prime Nutrition PhytoForm Fruits & Greens Formula recall affects 85,950 units distributed nationwide. Hi-Tech Pharmaceuticals Inc. will handle refunds or replacements. The product carries unapproved drug claims and is misbranded. Consumers who purchased this product should not consume it and should contact the company for refund or replacement information.

Prime Nutrition
Unapproved Drug
Read more
Food & Beverages
HIGH

Hi-Tech Pharmaceuticals Recalls PrimeNutrition PhytoForm Fruits & Greens Formula 30 Servings for Unf

Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition PhytoForm Fruits & Greens Formula dietary supplement on Aug. 6, 2025. The product was manufactured by Prime Nutrition and distributed nationwide. The recall cites unapproved drug claims and misbranding. Consumers should not use the product and should contact Hi-Tech Pharmaceuticals for refund or replacement.

Hi-Tech Pharmaceuticals
Unapproved Drug
Read more
Food & Beverages
HIGH

Hi-Tech Pharmaceuticals’ PrimeNutrition PhytoForm Fruits & Greens Recall for Unapproved Drug Claims

Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition PhytoForm Fruits & Greens Formula after FDA enforcement flagged unapproved drug claims and misbranding. The dietary supplement was distributed to 40+ states before the recall was issued on 2025-08-06 and remains active. Consumers should not consume the product and should seek refund or replacement from Hi-Tech Pharmaceuticals.

Hi-Tech Pharmaceuticals
Unapproved Drug
Read more