Food Recall Check
Class II · Moderate risk Ongoing Initiated May 12, 2021 (5 years ago)

Lipodrene With 25mg Ephedra Extract recall

Recalled by Hi Tech Pharmaceuticals · Norcross, GA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

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

The label gives no warning, so buyers cannot know about dangerous interactions with medicines they already take. All hidden drug ingredients recalls.

What was recalled

Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9

Quantity: 19,068/100 ct bottles

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 # 001211197, Exp. 12/25

Where it was sold

Alabama Arizona California Colorado Connecticut Florida Georgia Iowa Idaho Illinois Indiana Kansas Louisiana Massachusetts Maryland Maine Michigan Missouri Mississippi Montana North Carolina Nebraska New Jersey New Mexico Nevada New York Ohio Oklahoma Oregon Pennsylvania Puerto Rico Tennessee Texas Utah Virginia Vermont Washington Wisconsin

FDA's distribution note: The product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, VT, WA & WI.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away.

Recalling firm
Hi Tech Pharmaceuticals
Initiated by
Voluntary: Firm initiated
Recall initiated
May 12, 2021
In FDA report of
Jun 9, 2021
FDA recall number
F-0647-2021 · event 87919
Official record
FDA enforcement report search

Other recalls by Hi Tech Pharmaceuticals