Severity
Critical
CriticalClass IOngoing
FDA Drug recall · Reported June 18, 2025
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
Saini Trade INC recalled ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by H… - a critical-severity action.
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by H… was recalled by Saini Trade INC in June 18, 2025. Reason: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared pr…. Check the official notice for the remedy. Verify recall #D-0466-2025 with the FDA Drug before acting.
The recall
Saini Trade INC issued this critical-severity FDA Drug recall-Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared pr….
- Critical
- severity level
- Class I
- classification
- June 18, 2025
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0466-2025 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0466-2025) was formally reported on June 18, 2025, with the manufacturer initiating the action on April 14, 2025. It is classified under Critical severity (Class I), with a current status of Ongoing. Saini Trade INC is listed as the recalling firm, operating out of Tempe, AZ. Federal records list the affected scope as 500 boxes.
The documented reason for this recall is: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil. Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified high severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
500 boxes
Related Recalls
6
0 from same agency
Product description
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.
Reason for recall
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Critical (Class I) |
| Status | Ongoing |
| Recall number | D-0466-2025 |
| Date reported | June 18, 2025 |
| Date initiated | April 14, 2025 |
| Recalling firm | Saini Trade INC |
| Firm location | Tempe, AZ |
| Affected scope | 500 boxes |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0466-2025) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- This is a Class I (high-risk) recall, stop using the product immediately and follow the disposal or return instructions. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.. Recalled by Saini Trade INC. Units affected: 500 boxes.
Why was this product recalled? ▼
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 18, 2025. Severity: Critical. Recall number: D-0466-2025.
Where was the recalled product distributed? ▼
Distribution: Nationwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (D-0466-2025) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported June 18, 2025. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.