RAM IT Horny Goat Weed Dietary Supplement Recalled for Undeclared Sildenafil
Integrity Products recalls RAM IT Horny Goat Weed dietary supplement capsules nationwide because they contain undeclared sildenafil, a prescription drug not listed on the label.
The agency’s classification
FDA (Drugs): Class I
Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: FDA Class I classification requires a minimum severity score of 4 per the regulatory rubric. The undeclared presence of a pharmaceutical drug in a dietary supplement marketed without approval constitutes a serious regulatory violation, though no illnesses or injuries have been reported.
Plain-English summary
Integrity Products is recalling RAM IT Horny Goat Weed dietary supplement capsules because they contain undeclared sildenafil. Lot HGW221116 (Batch 020123-1), expiring May 31, 2025, is affected. The recall covers approximately 2,500 boxes distributed nationwide.
Sildenafil is a prescription pharmaceutical ingredient that was not disclosed on the product label. Federal regulations require dietary supplements containing drug ingredients to have FDA approval through a New Drug Application (NDA) or Abbreviated New Drug Application (ANDA) before marketing. This product was distributed without such approval.
Consumers who have purchased this product should stop using it immediately and consult a healthcare provider if they have consumed it.
The recalled product
- Product
- RAM IT, Horny Goat Weed, dietary supplement capsules, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026
- Manufacturer
- Integrity Products
- Category
- Drug — Dietary Supplement
- Affected units
- 2,500
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)
- Lot HGW221116 (Batch 020123-1)
- Exp 5/31/2025
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Integrity Products under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
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