USA LESS Inc. recalls LEOPARD Miracle Honey packaged in a wooden box, UPC 8 699415 910534, containing 12 sachets 180Gr / 6.36 Oz, each 1
USA LESS Inc. recalls LEOPARD Miracle Honey (UPC 8 699415 910534) due to undeclared sildenafil. This unapproved drug poses safety risks as it lacks FDA approval for erectile dysfunction treatment.
Recall notice
Marketed Without An Approved NDA/ANDA: product tainted with undeclared sildenafil, an FDA approved drug for the treatment of male erectile dysfunction. The presence of sildenafil in Leopard Miracle Honey renders it an unapproved drug for which safety and efficacy have not been established and, therefore, subject to recall.
Contact the company & request your remedy
What happened, in plain English
USA LESS Inc. is recalling LEOPARD Miracle Honey products because they contain undeclared sildenafil, an FDA-approved drug for erectile dysfunction. This makes the honey an unapproved product with unknown safety and effectiveness, potentially causing health risks. Read more at govinfonow.com/recall/39128-leopard-miracle-honey-recall-unapproved-sildenafil-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/39128-leopard-miracle-honey-recall-unapproved-sildenafil-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1135-2019
Cite this page
“LEOPARD Miracle Honey Recall: Unapproved Sildenafil Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39128-leopard-miracle-honey-recall-unapproved-sildenafil-risk. Based on FDA recall #D-1135-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1135-2019%22&limit=1).
Why it’s dangerous
The honey contains sildenafil, an FDA-approved drug for erectile dysfunction, but it's marketed without proper regulatory approval. This means safety and effectiveness haven't been tested, and the product could cause health issues.
Who’s affected
People who purchased LEOPARD Miracle Honey from USA LESS Inc. in Turkey. Those with pre-existing conditions or using the product for medical purposes may face higher risks.
How to tell if you have this one
Check for LEOPARD Miracle Honey in wooden boxes with UPC 8 699415 910534. Products sold in Turkey by USA LESS Inc. are affected.
- Brand
USA LESS- Product
LEOPARD Miracle Honey packaged in a wooden box, UPC 8 699415 910534, containing 12 sachets 180Gr / 6.36 Oz, each 1- Category
Drug
What to do — step by step
Check Product Details
Look for the UPC 8 699415 910534 on the wooden box packaging.
Questions people ask
Is this honey safe to consume?
The recall states the honey contains undeclared sildenafil, an unapproved drug. Safety and effectiveness have not been established, so it may pose health risks.
What should I do if I have this product?
The recall record does not specify a remedy, so no action is required beyond checking if you have the product.
Is this product dangerous for everyone?
The recall indicates potential health risks, especially for people with pre-existing conditions or those using the product for medical purposes.
Contact USA LESS
We’ve drafted a message you can send USA LESS to request your refund or repair — edit it as you like.
Subject: Recall D-1135-2019 — USA LESS LEOPARD Miracle Honey packaged in a wooden box, UPC 8 699415 910534, containing 12 sachets Hello, I own a LEOPARD Miracle Honey packaged in a wooden box, UPC 8 699415 910534, containing 12 sachets 180Gr / 6.36 Oz, each 1 that is covered by recall D-1135-2019 from USA LESS. 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-1135-2019 (March 5, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1135-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.