Class III · Low riskTerminated Initiated Jun 11, 2012 (14 years ago)
Fertalin bottles of 90 tablets taken orally Nokomis Research Inc… recall
Recalled by H & L Jerch Sales, Inc. · South Haven, MI, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
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.
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Catalog number: #8: UPC 771733109024; and lot numbers: 11157, 12103, 12221, and 12289.
Where it was sold
Nationwide.
FDA's distribution note: Nationwide
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
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…
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…
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…