# FDA recall D-0004-2025

> **Supercore Products Group Inc.** · Class I · drug recall initiated 2024-07-12.

## Product

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

## Reason for recall

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

## Distribution

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

## Key facts

- **Recall number:** D-0004-2025
- **Recalling firm:** Supercore Products Group Inc.
- **Classification:** Class I
- **Product type:** drug
- **Status:** Ongoing
- **Initiation date:** 2024-07-12
- **Report date:** 2024-10-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Atlanta, GA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0004-2025

## Citation

> AI Analytics. FDA recall D-0004-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/D-0004-2025. Source: US FDA. Licensed CC0.

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