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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94366

2 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
February 01, 2024
Product types
Drug
Classifications
Class I
Statuses
Ongoing
Recalling firm wording
Integrity Products

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

2 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 2

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

D-0585-2024
Recall number
D-0585-2024
Initiated
February 01, 2024
Classification
Class I
Status
Ongoing
Recalling firm
Integrity Products
Quantity
2500 boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot HGW221116 (Batch 020123-1), Exp 5/31/2025

Distribution pattern

Nationwide in the USA

drug · product 2 of 2

To the Moon Capsules, Horny Goat Weed, 1000 mg, packaged in a box containing a 10-count blister card, Distributed By: Integrity Products, 1710 Fenpark Dr., Fenton, MO 63026

D-0586-2024
Recall number
D-0586-2024
Initiated
February 01, 2024
Classification
Class I
Status
Ongoing
Recalling firm
Integrity Products
Quantity
2500 boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: Products contain undeclared sildenafil.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot HGW221116 (Batch 022123-1), Exp 5/31/2025

Distribution pattern

Nationwide in the USA