CLASS I ONGOING Drug recall · Reported 18 Jun 2025 · FDA Enforcement Report

Male Ultra, Unleash Your Force, Dietary Supplement recalled

Saini Trade is recalling Male Ultra, Unleash Your Force, Dietary Supplement per, distributed nationwide in the US. The recall was initiated on 14 Apr 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesAll Lots Lot #: KT-1ST-43-01-10-2025, Exp. 01/10/2027
Quantity recalled3000 boxes

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0463-2025
FDA event ID
96735
Recalling firm
Saini Trade, Tempe, AZ
Classification
Class I
Status
Ongoing
Recall initiated
14 Apr 2025
FDA classified
11 Jun 2025
Reported
18 Jun 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Labeling Errors

Timeline

14 Apr 2025Recall initiated by company
11 Jun 2025Classified by FDA+58 days
18 Jun 2025Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.

Product as listed by the FDA

Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, UPC B0CMQ4FTHG.

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Is Male Ultra, Unleash Your Force, Dietary Supplement per recalled?

Yes. Saini Trade recalled Male Ultra, Unleash Your Force, Dietary Supplement per on 14 Apr 2025. The recall is Class I and its status is Ongoing. Recall number D-0463-2025.

Why was it recalled?

Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.

Which lots are affected?

All Lots Lot #: KT-1ST-43-01-10-2025, Exp. 01/10/2027

Where was it sold?

Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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