Dietary Supplement ULTRA ARMOR Recalled for Undeclared Drug Ingredients
ULTRA ARMOR dietary supplement, distributed by Health Fixer, is recalled nationwide because it contains undeclared pharmaceutical ingredients propoxyphenylsildenafil and sildenafil. The product was marketed without FDA approval.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The FDA classified this as a Class I recall. Per the rubric, FDA Class I recalls must score no lower than 4. The presence of undeclared pharmaceutical active ingredients in a product marketed as a dietary supplement creates a serious health risk due to potential drug interactions and unintended adverse effects.
Plain-English summary
ULTRA ARMOR, My Armor My Power dietary supplement in 10-capsule boxes (UPC B0CYJ7Y5H9) distributed by Health Fixer, Tempe, AZ 85288, is being recalled nationwide. Lot #KT-1ST-43-01-10/2025 (Exp. 01/10/2027) was found through laboratory analysis to contain undeclared propoxyphenylsildenafil and sildenafil, both pharmaceutical active ingredients.
The product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA) from the FDA. The presence of undeclared pharmaceutical ingredients in a dietary supplement product poses a safety risk to consumers who may be unaware they are ingesting prescription-strength drugs, which could interact with other medications or cause adverse effects.
Consumers who have purchased this product should stop using it immediately and dispose of it safely. Consumers with questions or who have experienced any adverse effects should contact their healthcare provider.
The recalled product
- Product
- ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.
- Manufacturer
- SAINI TRADE INC
- Category
- Drug — Dietary Supplement
- Hazard
- undeclared-drug-ingredient
- propoxyphenylsildenafil
- sildenafil
- unapproved-nda
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- All lots Lot #: KT-1ST-43-01-10/2025
- Exp. 01/10/2027
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- HighROHTO Cooling Eye Drops Recalled Over Sterility Assurance Concerns
FDA (Drugs) · 2026-07-29
- HighLEVOTHYROXINE SODIUM Tablets Recalled Due to Subpotent Drug Content
FDA (Drugs) · 2026-07-29
- SevereFDA Recalls Rohto Dry-Aid Eye Drops Over Sterility Assurance Gap
FDA (Drugs) · 2026-07-29
- SevereDietary Supplement Modern Warrior Ready Recalled for Unapproved Ingredients
FDA (Food) · 2026-07-29
- HighBeak & Skiff Alcohol Antiseptic Sanitizer recalled for acetaldehyde contamination
FDA (Drugs) · 2026-07-29