LOW RISK Terminated F-1731-2012

Fertalin bottles of 90 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #8

Recalled by H & L Jerch Sales, Inc.

Classification

Class III — Products that are unlikely to cause any adverse health reaction, but that violate FDA labeling or manufacturing laws.

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.

Product Details

Product Quantity
688 bottles
Product Type
Food
Code Info
Catalog number: #8: UPC 771733109024; and lot numbers: 11157, 12103, 12221, and 12289.
Voluntary/Mandated
Voluntary: Firm initiated

Distribution & Geography

Distribution Pattern
Nationwide
Company Location
South Haven, MI, 49090-8119

Timeline

Report Date
07/18/2012
Recall Initiated
06/11/2012
Classification Date
07/06/2012
Termination Date
02/12/2013

Source: U.S. Food & Drug Administration (FDA) — FDA Recalls

Last updated: August 28, 2026

Get Real-Time Recall Alerts on Your Phone

Scan any grocery receipt and instantly know if your food has been recalled. Free download — protect your family in 3 seconds.