Product Name: Eroxil bottles of 30 tablets taken orally Nokomis… — Class III food recall F-1729-2012
Terminated recall by H & L Jerch Sales, Inc., reported 2012-07-18, distributed nationwide. The products contain synthetic equivalents of spermine and/or spermidine, which are constituents or extracts o
| Recall number | F-1729-2012 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | H & L Jerch Sales, Inc., South Haven, MI, United States |
| Recall initiated | 2012-06-11 |
| Classified | 2012-07-06 |
| Reported by FDA | 2012-07-18 |
| Terminated | 2013-02-12 |
| Distributed | Nationwide (US) |
| Quantity | 50,604 bottles |
| UPC / GTIN / UDI-DI | 00771733109000 |
| Lot numbers | 11154, 11185, 11186, 11267, 11269, 12014, 12057, 12099, 12220, 12244 |
Product
Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6
Reason for recall
The products contain synthetic equivalents of spermine and/or spermidine, which are constituents or extracts of an herb or other botanical, and the that a synthetic copy of a constituent or extract of an herb or other botanical is not a dietary ingredient, and such ingredients must be approved for use in supplements. The use has not been approved.
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/F-1729-2012. 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.