FDA Drugs recall ·
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box… recall
This is an FDA Class I recall — the most serious type.
- Recall number
- D-0466-2025
- Date
- (initiated April 14, 2025)
- Company / brand
- Saini Trade Inc
1405 N Scottsdale Rd, Tempe, AZ, United States - Category
- Drugs › Class I
- Classification
- Class I
- Status
- Ongoing
- Units affected
- 500 boxes
- Hazard tags
- Undeclared allergen
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.
Why was it recalled?
Marketed without an Approved NDA/ANDA: Laboratory analysis found the product to be tainted with undeclared propoxyphenylsildenafil and sildenafil.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
All lots Lot #: KT-1ST-43-01-10/2025, Exp. 01/10/2027
Distribution
Nationwide
What does Class I mean?
Class I is the most serious FDA recall class: there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Source: FDA (drugs), recall D-0466-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.