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Unrated Drug recall · FDA · Published August 18, 2021

Phe Inc X Rated Honey For Men Recall: Tainted with Tadalafil

Phe Inc recalls X Rated Honey For Men (15g packets) due to contamination with tadalafil. All lots expired 12/2025. No remedy specified in official notice.

🇺🇸 FDA recall #D-0819-2021DrugPhe Inc ›
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Recalling firmPhe Inc302 Meadowlands Dr · Hillsborough, NC 27278-8502
✎ GovInfoNow plain-language explainer

Phe Inc is recalling X Rated Honey For Men products because they were found to contain tadalafil. This contamination poses a health risk as tadalafil is a prescription drug. Consumers should avoid using these products until further notice. Read more at govinfonow.com/recall/35932-phe-inc-x-rated-honey-for-men-recall-tainted-with.

Source Summary by GovInfoNow · govinfonow.com/recall/35932-phe-inc-x-rated-honey-for-men-recall-tainted-with · Updated August 18, 2026 · FDA enforcement record: FDA #D-0819-2021

Cite this page

“Phe Inc X Rated Honey For Men Recall: Tainted with Tadalafil.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35932-phe-inc-x-rated-honey-for-men-recall-tainted-with. Based on FDA recall #D-0819-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0819-2021%22&limit=1).

The FDA announced on August 18, 2021, that Phe Inc voluntarily recalled X RATED HONEY FOR MEN due to undeclared Tadalafil. The drug was marketed without an approved New Drug Application or Abbreviated New Drug Application.

How to tell if you have it

  • Brand: Phe Inc
  • Product: X RATED HONEY FOR MEN
  • Packaging: 15g packets, 4 packets per box
  • UPC: 6 13682 41232 2
  • Lot/Expiration: All lots, Exp. 12/2025

The hazard

The product was found to be tainted with Tadalafil and marketed without an approved NDA or ANDA. The FDA classified this as a Class I recall.

Context

GovInfoNow's records show other recent recalls of similar products include StuffbyNainax MR 7 SUPER 700000 Capsules (2025-12-15) and Shoolin Pharma Chem Tadalafil 500g Recall (2026-08-03).

How to tell if you have this one

Check for the UPC code 6 13682 41232 2 on the packaging. The product comes in 15g packets, 4 per box, and expires by December 2025.

  • Brand
    Phe Inc
  • Product
    X RATED HONEY FOR MEN, packaged in 15g packets, 4 packets per box, UPC 6 13682 41232 2
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Look for the UPC code 6 13682 41232 2 on the packaging to confirm if it's recalled.

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 within the United States” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA published this recall 42 days after the firm started it.

1. Firm started the recall: Aug 18, 202112. FDA classified it Class I: Sep 21, 202123. Published in FDA’s Enforcement Report: Sep 29, 202132021
  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.

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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-0819-2021 (August 18, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0819-2021 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