LEOPARD Miracle Honey packaged in a wooden box — Class I drug recall D-1135-2019
Terminated recall by USA LESS Inc., reported 2019-04-17, distributed nationwide. Marketed Without An Approved NDA/ANDA: product tainted with undeclared sildenafil, an FDA approved drug for th
| Recall number | D-1135-2019 |
|---|---|
| Product type | Drug |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | USA LESS Inc., Brooklyn, NY, United States |
| Recall initiated | 2019-03-05 |
| Classified | 2019-04-16 |
| Reported by FDA | 2019-04-17 |
| Terminated | 2024-01-10 |
| Distributed | Nationwide (US) |
| Quantity | 83 boxes |
| Reason classes | undeclared allergen, unapproved product |
Product
LEOPARD Miracle Honey packaged in a wooden box, UPC 8 699415 910534, containing 12 sachets 180Gr / 6.36 Oz, each 1 Sachet 15 gr / 0.53 Oz is labeled as LEOPARD Miracle of Honey, UPC 8 699415 912859, Manufactured in Turkey, www leopardhoneytr.com.
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1135-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.