Food Recall Check
Class III · Low risk Terminated Initiated Aug 6, 2025 (14 months ago)

Hi-Tech Pharmaceuticals L-Glutamine Ultra Pure Powder Hplc… recall

Recalled by Hi-Tech Pharmaceuticals Inc. · Norcross, GA, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Unapproved Drug Claims.

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

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 PHARMECEUTICALS, INC. 6015-B Unity Drive Norcross, GA 30071

Quantity: 85,950 units total

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot 059960809 Exp Date 06/28

Where it was sold

Alabama Arkansas Arizona California Colorado Connecticut Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland Michigan Minnesota Missouri Mississippi Montana North Carolina North Dakota Nebraska New Hampshire New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Rhode Island South Carolina South Dakota Tennessee Texas Utah Virginia Vermont Washington Wisconsin West Virginia Wyoming

FDA's distribution note: 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.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Hi-Tech Pharmaceuticals Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 6, 2025
In FDA report of
Sep 24, 2025
Terminated
Feb 19, 2026
FDA recall number
H-0591-2025 · event 97373
Official record
FDA enforcement report search

Also recalled with it (15 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Showing 12 of 15.

Other recalls by Hi-Tech Pharmaceuticals Inc.

Class II · Moderate risk Ongoing Hidden drug

Lipodrene With 25mg Ephedra Extract

Reason The firm was notified by the FDA that the product contains the unapproved food additive 1,4-dimethylamylamine (DMAA).

Hi Tech Pharmaceuticals 38 states F-0647-2021