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Stop using now Drug recall · FDA · Published February 9, 2022

Walmart recalls Avaphinal pills with undeclared sildenafil - unapproved drug risk

Walmart recalls Avaphinal Maximum Male Enhancement pills containing undeclared sildenafil, an unapproved drug ingredient. Consumers should stop using these pills as they are not FDA approved.

🇺🇸 FDA recall #D-0725-2022DrugWalmart Stores ›
Take action

Contact the company

Official pagewww.walmart.com
Recalling firmWalmart Stores805 Moberly Ln · Bentonville, AR 72716-0560
✎ GovInfoNow plain-language explainer

Walmart is recalling Avaphinal Maximum Male Enhancement pills that contain undeclared sildenafil, an ingredient approved for other male sexual health treatments. This makes the product an unapproved drug, which could pose health risks if used without proper medical oversight. Read more at govinfonow.com/recall/35228-walmart-recalls-avaphinal-pills-with-undeclared-sildenafil-unapproved-drug-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/35228-walmart-recalls-avaphinal-pills-with-undeclared-sildenafil-unapproved-drug-risk · Updated August 18, 2026 · FDA enforcement record: FDA #D-0725-2022

Cite this page

“Walmart recalls Avaphinal pills with undeclared sildenafil - unapproved drug risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35228-walmart-recalls-avaphinal-pills-with-undeclared-sildenafil-unapproved-drug-risk. Based on FDA recall #D-0725-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0725-2022%22&limit=1).

Walmart Stores recalled Avaphinal Maximum Male Enhancement Sexual Pills nationwide on Feb. 9, 2022, according to the FDA. The product was found to contain undeclared sildenafil, an ingredient in approved drugs for male sexual enhancement.

How to tell if you have it

  • Brand: Walmart Stores
  • Product: Avaphinal Maximum Male Enhancement Sexual Pills, 2000 MG*
  • Packaging: 10 Capsules per carton
  • Lot code: DK1027
  • Expiration date: 08/01/2023
  • Sold via www.walmart.com

The hazard

The FDA classified the product as an unapproved drug because it contained undeclared sildenafil. This ingredient is found in FDA-approved products for the treatment of male sexual enhancement.

Context

GovInfoNow's records show Walmart Stores has issued other recalls, including one on Dec. 15, 2025, for StuffbyNainax MR 7 SUPER 700000 Capsules due to undeclared sildenafil and tadalafil. Other recent recalls of similar products include Buy-Herbal Kian Pee Wan Capsules Recall (March 21, 2026) and SUN PHARMACEUTICAL Xyvona 3mg Tablets Recall (May 22, 2026).

How to tell if you have this one

Check for the product name 'Avaphinal Maximum Male Enhancement Sexual Pills' and the lot number DK1027 with expiration date 08/01/2023. The product comes in 10 capsules per carton.

  • Brand
    Walmart Stores
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Stop Using Now

    Immediately stop using the recalled Avaphinal pills as they contain undeclared sildenafil, an unapproved drug ingredient.

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 via www.walmart.com” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 10 months after the firm started it.

1. Firm started the recall: Feb 9, 202212. Published in FDA’s Enforcement Report: Mar 23, 202223. FDA classified it Class I: Mar 29, 202234. FDA terminated the recall: Dec 2, 202242022
  1. Firm started the recall
  2. Published in FDA’s Enforcement Report
  3. FDA classified it Class I
  4. FDA terminated the recall

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

Take action

Contact Walmart Stores

We’ve drafted a message you can send Walmart Stores to request your refund or repair — edit it as you like.

Subject: Recall D-0725-2022 — Walmart Stores Walmart recalls Avaphinal pills with undeclared sildenafil - unapproved drug risk

Hello,

I own a Walmart recalls Avaphinal pills with undeclared sildenafil - unapproved drug risk that is covered by recall D-0725-2022 from Walmart Stores.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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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-0725-2022 (February 9, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0725-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 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