hi-tech pharmaceuticals inc.foodHigh PriorityExpired

HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE SIZE POWER RECOVERY ENERGY STRENGTH LACTIC ACIDE ELIMINATION LEAN MUSCLE 500 GRAMS NET WT. (17.630OZ) DIETARY SUPPLEMENT UPC 8 11836 02362 6 HI-TECH

hi-tech pharmaceuticals inc. HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE SIZE POWER RECOVERY ENERGY STRENGTH LACTIC ACIDE ELIMINATION LEAN MUSCLE 500 GRAMS NET WT. (17.630OZ) DIETARY SUPPLEMENT UPC 8 11836 02362 6 HI-TECH was recalled by the FDA. Unapproved Drug Claims.

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 L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE SIZE POWER RECOVERY ENERGY STRENGTH LACTIC ACIDE ELIMINATION LEAN MUSCLE 500 GRAMS NET WT. (17.630OZ) DIETARY SUPPLEMENT UPC 8 11836 02362 6 HI-TECH was recalled by the FDA. Unapproved Drug Claims.

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This recall is no longer active. You can still review details here for historical reference and confirmation.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 L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE SIZE POWER RECOVERY ENERGY STRENGTH LACTIC ACIDE ELIMINATION LEAN MUSCLE 500 GRAMS NET WT. (17.630OZ) DIETARY SUPPLEMENT UPC 8 11836 02362 6 HI-TECH Agency: FDA | Category: food | Date: 2025-08-06 Reason: Unapproved Drug Claims. 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.

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

Lot 059960809 Exp Date 06/28

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 059960809 Exp Date 06/28.

What is the remedy for this recall?

## HI-TECH PHARMACEUTICALS L-GLUTAMINE ULTRA PURE POWDER HPLC VERIFIED 99.5% PURITY CELL VOLUMIZATION MUSCLE SIZE POWER RECOVERY ENERGY STRENGTH LACTIC ACIDE ELIMINATION LEAN MUSCLE 500 GRAMS NET WT. (17.630OZ) DIETARY SUPPLEMENT UPC 8 11836 02362 6 HI-TECH Agency: FDA | Category: food | Date: 2025-08-06 Reason: Unapproved Drug Claims. 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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