← FDA ENFORCEMENT
D-0004-2025Class I

Supercore Products Group Inc.

Recalling firm
Supercore Products Group Inc.
Product type
Drug
Status
Ongoing
Report date
2024-10-09
Distribution
Nationwide US (2014), Israel (2), Canada (12), Republic of Kosovo (1), Pakistan (1), Australia (3), Morocco (1), United Kingdom (1)
Firm state
GA
Product quantity
615
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Documentation & Change Control
Reason for recall

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

Product description

Gold Hard Steel Plus Liquid, 2 FL OZ bottles, UPC 787188873199

Code / lot info

All lots

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.