Supercore Products Group Inc.: Drug Recall

Recall #D-0003-2025 · 07/12/2024

Class I: Dangerous

Recall Details

Recall Number: D-0003-2025
Classification: Class I
Product Type: Drug
Recalling Firm: Supercore Products Group Inc.
Status: Ongoing
Date Initiated: 07/12/2024
Location: Atlanta, GA, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 729

Reason for Recall

Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.

Product Description

Hard Steel Capsules packaged in 1 count blister packs in boxes of 10, 20 and 30, Manufactured in U.S.A.

Distribution Pattern

Nationwide US (2014), Israel (2), Canada (12), Republic of Kosovo (1), Pakistan (1), Australia (3), Morocco (1), United Kingdom (1)

Other Recalls by Supercore Products Group Inc.

Class I: Dangerous 07/12/2024

Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.

View all recalls by Supercore Products Group Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.