Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6
Recalling firm: H & L Jerch Sales, Inc.
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…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Feb 12, 2013.
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771733109000FDA code information
Catalog number: #6: UPC 771733109000; and lot numbers: 11154, 11185, 11186, 11267, 11269, 12014, 12057, 12099, 12220, and 12244.
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Full FDA record and distribution details
Original product description
Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 771733109000 | Catalog number: #6: UPC 771733109000; and lot numbers: 11154, 11185, 11186, 11267, 11269, 12014, 12057, 12099, 12220, and 12244. |
Original FDA recall reason
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.
Recall details
- Recall number
- F-1729-2012
- Event ID
- 61842
- FDA status
- Terminated
- Initiated
- Jun 11, 2012
- Reported
- Jul 18, 2012
- Classified
- Jul 6, 2012
- Terminated
- Feb 12, 2013
- Quantity
- 50,604 bottles
- Location
- South Haven, MI, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
Nationwide
Data updated September 16, 2026. View official FDA data ↗
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