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FDA

HI-TECH PHARMACEUTICALS ADDEREX XR STRONGEST FOCUSING AID WITHOUT A PRESECRIPTION! HELPS ADULTS MAINTAIN CONCENTRATION & IMPROVE PRODUCTIVITY! 30 TABLETS UPC 8 11836 02691 7 HI-TECH PHARMACEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071

Published: Aug 6, 2025
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Updated: Nov 4, 2025
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Recall #: H-0587-2025
Product Information

Brand

Hi-Tech Pharmaceuticals Inc.

Category

Food

Description

Unapproved Drug Claims and Misbranded.

FDA Classification

Class III

Not likely to cause adverse health consequences

Status

Ongoing

Recall Type

Voluntary: Firm initiated

Affected Lot Codes

Check your product packaging for these codes:

Lot 303120691 Exp Date 05/28

Affected States/Regions

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

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.

What You Should Do

Available Remedies

Dispose of ProductRefund Available

Recommended Actions

  1. 1Stop using the product immediately. Do not continue to use, sell, or distribute the recalled product.
  2. 2Check if you have the recalled product. Verify the brand, model number, lot codes, or UPC listed in the recall.
  3. 3Follow the remedy instructions. Return the product to the place of purchase for a full refund. Dispose of the product safely according to local regulations.
  4. 4Visit the official recall page for complete details, contact information, and deadline information (if applicable).

Official Recall Information

For the most accurate and up-to-date information, including contact details and deadlines, please visit the official recall page from FDA.

View Official Recall Page

Need more help? If you have questions or have experienced issues with this product, you can:

  • Contact the manufacturer or retailer where you purchased the product
  • Report an incident to SaferProducts.gov
  • Consult with the FDA for additional guidance