Recall Overview

Iovate Health Sciences USA Inc. has initiated a voluntary recall of a dietary supplement product due to the presence of an undeclared substance. The recall is currently ongoing and affects both domestic and international markets.

Product Details

Product Name: Alpha Test 120 count

Classification: Class II

Recall Status: Ongoing

Reason for Recall

The recall was initiated due to the presence of cathine in the product. Cathine is a stimulant that can have various effects on the body. You can learn more about cathine on .Wikipedia

Health Risks

The presence of cathine may pose health risks, especially to individuals sensitive to stimulants. Consumers may experience increased heart rate, elevated blood pressure, or other adverse effects.

Distribution & Affected Areas

The product was distributed across various states in the United States, including NC, CA, TX, NJ, VA, NV, PA, IN, NY, CA, IL, MS, KY, MI, SC, WA, CT, FL, OH, WI, DE, LA, TN, MO, UT, KH, GA, KS, CO, IA, AZ, OR. Additionally, it was distributed internationally to South Africa (ZA), Philippines (PH), Israel (IS), Kazakhstan (KZ), and the United Arab Emirates (AE).

Action Required

Consumers who have purchased the affected product should discontinue use immediately and return it to the place of purchase for a refund. If you have any health concerns, please consult a healthcare professional.

Additional Information

Recall Initiation Date: December 18, 2024

Expiration Date and Lot Codes: March 21, 2027 (Lots 24A125, 24B059, 24B060), March 22, 2027 (Lot 24C112), July 3, 2027 (Lots 24F164, 24G112), July 4, 2027 (Lot 24E288), July 5, 2027 (Lots 24G243, 24H207)

Total Quantity Recalled: 163,248 units

Reference

For further details, please visit the .FDA's recall page

Contact Information

For any inquiries, you may contact Iovate Health Sciences USA Inc. at their Wilmington, DE address:

1105 N Market St Ste 1330, Wilmington, DE 19801-1241, United States.