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Class IOngoing

Gold Hard Steel Plus Liquid recall

FDA recall D-0004-2025 · initiated Jul 12, 2024

By the pharmaranks editorial teamReviewed against the FDA (openFDA) sourcesUpdated Oct 9, 2024How we research

Supercore Products Group Inc. recalled Gold Hard Steel Plus Liquid in Jul 2024 — an FDA Class I recall (D-0004-2025) because Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.

Most serious — a reasonable probability that use will cause serious harm or death.

Why it was recalled

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

Sold unapproved, or found to contain something undeclared

The product should not have been on sale in this form — often a supplement found to contain a hidden prescription drug.

This is a manufacturing or quality failure, not a finding that the medicine is unsafe to take — across every recall we hold, none was issued for that reason. It does not mean the batch was harmless.

Is your product affected? Check the lot number

A recall covers only specific lots. Find the lot number and expiration date on your package and compare them to the affected codes below — if yours is not listed, it was not part of this recall.

All lots

Quantity recalled: 615

Details

Product
Gold Hard Steel Plus Liquid, 2 FL OZ bottles, UPC 787188873199
Recalling company
Supercore Products Group Inc.
Classification
Class I
Status
Ongoing
Type
Voluntary: Firm initiated
Distribution
Nationwide US (2014), Israel (2), Canada (12), Republic of Kosovo (1), Pakistan (1), Australia (3), Morocco (1), United Kingdom (1)
Initiated
Jul 12, 2024
FDA report date
Oct 9, 2024
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.

Frequently asked

Was Gold Hard Steel Plus Liquid recalled?
Supercore Products Group Inc. recalled Gold Hard Steel Plus Liquid in Jul 2024 — an FDA Class I recall (D-0004-2025) because Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil. Most serious — a reasonable probability that use will cause serious harm or death.
Why was Gold Hard Steel Plus Liquid recalled?
Per the FDA enforcement record, the reason for recall D-0004-2025 was: Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Is a recalled Gold Hard Steel Plus Liquid dangerous to take?
An FDA recall removes specific lots from the market for a defined reason and does not by itself mean the medicine is unsafe for everyone — your specific lot may never have been affected. Most serious — a reasonable probability that use will cause serious harm or death. Check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This reproduces public FDA data and is not medical advice.
Which lots of Gold Hard Steel Plus Liquid are affected?
Distributed: Nationwide US (2014), Israel (2), Canada (12), Republic of Kosovo (1), Pakistan (1), Australia (3), Morocco (1), United Kingdom (1). The recall covers these lots — All lots. Check the lot number and expiration date on your package against this list; if yours is not listed, it was not part of recall D-0004-2025.

Source: openFDA Drug Enforcement record D-0004-2025

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