Skip to content
Get alerts
GovInfoNow
Stop using now Drug recall · FDA · Published February 1, 2024

Integrity Products Recalls RAM IT Dietary Supplements Due to Sildenafil

Integrity Products recalls RAM IT and Horny Goat Weed capsules due to undeclared sildenafil. Check your lot number HGW221116 for details.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-0585-2024DrugIntegrity Products ›
Take action

Contact the company

Recalling firmIntegrity Products5613 Park Road Suite 2 · High Ridge, MO 63049
✎ GovInfoNow plain-language explainer

Integrity Products is recalling RAM IT and Horny Goat Weed dietary supplement capsules because they contain undeclared sildenafil, a prescription drug ingredient not listed on the label. This recall affects approximately 2,500 boxes distributed nationwide in the USA. The product was marketed without an approved New Drug Application (NDA) or Abbreviated New Drug Application (ANDA). Read more at govinfonow.com/recall/32841-integrity-products-recalls-ram-it-dietary-supplements-due-to-sildenafil.

Source Summary by GovInfoNow · govinfonow.com/recall/32841-integrity-products-recalls-ram-it-dietary-supplements-due-to-sildenafil · Updated October 9, 2026 · FDA enforcement record: FDA #D-0585-2024

Cite this page

“Integrity Products Recalls RAM IT Dietary Supplements Due to Sildenafil.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/32841-integrity-products-recalls-ram-it-dietary-supplements-due-to-sildenafil. Based on FDA recall #D-0585-2024 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0585-2024%22&limit=1).

Integrity Products voluntarily recalled RAM IT Horny Goat Weed Capsules nationwide due to undeclared sildenafil, according to the FDA on Feb. 1, 2024.

How to tell if you have it

  • Brand: Integrity Products
  • Product: RAM IT Horny Goat Weed Capsules
  • Lot code: HGW221116 (Batch 020123-1)
  • Expiration date: 5/31/2025
  • Quantity: 2500 boxes

The hazard

The FDA classified the recall as Class I because the dietary supplement capsules were marketed without an approved New Drug Application or Abbreviated New Drug Application and contained undeclared sildenafil.

Context

Other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15) and Shoolin Pharma Chem Sildenafil Recall (2026-08-03). Buy-Herbal Kian Pee Wan Capsules were also recalled on 2026-03-21 for undeclared drug ingredients.

How to tell if you have this one

Look for boxes of RAM IT or Horny Goat Weed dietary supplement capsules, 1000 mg, packaged in a box containing a 10-count blister card. Check the lot number HGW221116 (Batch 020123-1) and expiration date 5/31/2025 to confirm if your product is affected.

  • Brand
    Integrity Products
  • Category
    Drug
FDA recall event · 2 products

All 2 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class I
  • Status
    Ongoing
  • Distribution
    Nationwide in the USA
Recall numberProduct, codes & lots
D-0585-2024RAM 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; Lot HGW221116 (Batch 020123-1), Exp 5/31/2025
D-0586-2024To 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; Lot HGW221116 (Batch 022123-1), Exp 5/31/2025
Based on the official FDA remedy

What to do — step by step

  1. Stop using the product

    Do not consume any capsules from the recalled boxes due to the risk of undeclared sildenafil exposure.

  2. Discard or return the item

    The recall record does not specify a specific remedy such as a refund or replacement, so consumers should dispose of the product safely.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the USA” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 5 months after the firm started it.

1. Firm started the recall: Feb 1, 202412. FDA classified it Class I: Jul 3, 202423. Published in FDA’s Enforcement Report: Jul 10, 202432024
  1. Firm started the recall
  2. FDA classified it Class I
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

Similar recalls

One Source Vitality Recall: Undeclared Sildenafil Hazard
One Source NutritionAPEXXX 300mg Tablet Recall: Hidden Sildenafil Hazard
APEXXXStuffbyNainax MR 7 SUPER 700000 Capsules: FDA Finds Undeclared Sildenafil and Tadalafil
StuffbyNainaxApotex Recalls Paroxetine 37.5mg Due to Dissolution Failure
Apotex Corp.Ajanta Pharma Recalls Ranolazine 1000mg Due to Dissolution Failure
Ajanta Pharma USA Inc

Latest drug recalls

Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company recalls Clear Eyes Redness Relief, Lubricant/Redness Reliever Eye Drops (glycerin 0.25%, naphazoline hydrochloride 0.012%) with
Insight Pharmaceuticals · September 15, 2026Amneal Pharmaceuticals, LLC recalls Estradiol Gel, 0.1%, 0.25 mg, 30-packets per carton, Rx only, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater,
Amneal Pharmaceuticals · September 8, 2026Inventia Healthcare Limited recalls Chlorthalidone Tablets, USP, 25 mg, 100 Tablets per bottle, Rx only, Manufactured by: Inventia Healthcare Limited. NDC:
Inventia Healthcare · September 3, 2026SV Labs Toronto Corporation recalls Benzoyl Peroxide Wash, USP, 10%, packaged in a)5 FL OZ (148mL) bottles (NDC 0536-1261-63), and b) 8.5 FL OZ (237 mL)
SV Labs · September 1, 2026SUN PHARMA /TARO recalls Lidocaine Ointment USP, 5%, Speermint Flavor, 50 g Jar, Rx only, Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario,
SUN PHARMA /TARO · August 31, 2026Supernus Pharmaceuticals, Inc. recalls Trokendi XR, (topiramate) extended-release capsules, 50 mg, 30 Capsules, Rx only, Manufactured by: Catalent Pharma
Supernus Pharmaceuticals · August 31, 2026

Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0585-2024 (February 1, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0585-2024 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA