hi-tech pharmaceuticals inc.foodHigh PriorityExpired

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

hi-tech pharmaceuticals inc. 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 was recalled by the FDA. Unapproved Drug Claims and Misbranded.

By RecallRadar Editorial Team

Sourced from FDA. Last reviewed March 4, 2026.

This recall involves safety concerns. Take action promptly.

Plain-English Summary

hi-tech pharmaceuticals inc. 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 was recalled by the FDA. Unapproved Drug Claims and Misbranded.

Is This Recall Still Active?

Status: No - Expired

This recall is no longer active. You can still review details here for historical reference and confirmation.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source
FDA
Announced by source
August 6, 2025
Last reviewed by RecallRadar
March 4, 2026

What You Should Do

  1. 1## 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 Agency: FDA | Category: food | Date: 2025-08-06 Reason: Unapproved Drug Claims and Misbranded. What to do:
  2. 2Stop using the product if it matches your lot/model.
  3. 3Compare your product details with the FDA recall notice.
  4. 4Follow the manufacturer's remedy instructions (refund, replacement, or disposal).
Open Official Recall NoticeMake sure you're covered for future hi-tech pharmaceuticals inc. recalls

What's Being Recalled

Quoted source excerpt from the official notice.

Unapproved Drug Claims and Misbranded.

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

Lot 303120691 Exp Date 05/28

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

Frequently Asked Questions

Is my hi-tech pharmaceuticals inc. device affected?

Check the affected models section on this page. The official notice currently lists Lot 303120691 Exp Date 05/28.

What is the remedy for this recall?

## 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 Agency: FDA | Category: food | Date: 2025-08-06 Reason: Unapproved Drug Claims and Misbranded. What to do: 1. Stop using the product if it matches your lot/model. 2. Compare your product details with the FDA recall notice. 3. Follow the manufacturer's remedy instructions (refund, replacement, or disposal).

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Keep browsing with these internal hubs: hi-tech pharmaceuticals inc. recall hub and Food & Drug recall hub.

Official Resources

Use these primary sources for final eligibility and claim instructions.

View official notice from FDA

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Quick Info

Brand
hi-tech pharmaceuticals inc.
Category
food
Source Agency
FDA
Announced
August 6, 2025
Country
US
Status
Expired

Source & Verification

Sourced from FDA. Last reviewed March 4, 2026.

Official source
FDA
Announced by source
August 6, 2025
Last reviewed by RecallRadar
March 4, 2026

Official Resources

Use these primary sources for final eligibility and claim instructions.

Open Official Recall NoticeView official notice from FDA

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