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
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Food Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 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
- Dietary Supplement (Joint Support)
- Model numbers
- Lot 503110607 Exp Date 04/30
- Sizes
- 90CT
- Sold at
- Unknown
- Where affected
- Nationwide
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
August 6, 2025
Reported by FDA FOOD
September 24, 2025
RecallRadar source check
April 18, 2026
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
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
- Check product label for UPC 8 57084 00035 4 and Lot 503110607 Exp 04/30
- Verify package shows Joint-RX 600mcg and 90CT
- 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
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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
- Shipped to 40+ states including CA, FL, GA, NY
- Active recall as of 2025-08-06 with report dated 2025-09-24
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
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