FDA recall record
Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of February 12, 2013. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6
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.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6
Code information listed by FDA
Catalog number: #6: UPC 771733109000; and lot numbers: 11154, 11185, 11186, 11267, 11269, 12014, 12057, 12099, 12220, and 12244.
Distribution and firm information
Recalling firm listed by FDA: H & L Jerch Sales, Inc.
Firm location listed by FDA: South Haven, MI, United States
Distribution reported by FDA: Nationwide
Product quantity listed by FDA: 50,604 bottles
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.