FDA recall record

Integrity Products RAM IT, Horny Goat Weed, dietary supplement capsules, 1000 mg recall — FDA D-0585-2024

Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

Class Iclassification
D-0585-2024official record ID
Jul 10, 2024report date

Recall record at a glance

Official recordD-0585-2024
CategoryDrug Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmIntegrity Products
Report dateJul 10, 2024
Recall initiation dateFeb 1, 2024
Quantity2500 boxes
LocationHigh Ridge, MO, United States

Official product description

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

Why the product was recalled

Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

Distribution information

Nationwide in the USA

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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