CLASS III Food recall · Reported 18 Jul 2012 · FDA Enforcement Report

Eroxil bottles of taken orally Nokomis Research Inc #6 recalled

H & L Jerch Sales is recalling Eroxil bottles of taken orally Nokomis Research Inc #6, distributed nationwide in the US. The recall was initiated on 11 Jun 2012 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesCatalog number: #6: UPC 771733109000; and lot numbers: 11154, 11185, 11186, 11267, 11269, 12014, 12057, 12099, 12220, and 12244.
Quantity recalled50,604 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1729-2012
FDA event ID
61842
Recalling firm
H & L Jerch Sales, South Haven, MI
Brand
Eroxil
Classification
Class III
Status
Terminated
Recall initiated
11 Jun 2012
FDA classified
6 Jul 2012
Reported
18 Jul 2012
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Other

Timeline

11 Jun 2012Recall initiated by company
6 Jul 2012Classified by FDA+25 days
18 Jul 2012Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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 as listed by the FDA

Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it 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.

Which lots are affected?

Catalog number: #6: UPC 771733109000; and lot numbers: 11154, 11185, 11186, 11267, 11269, 12014, 12057, 12099, 12220, and 12244.

Where was it sold?

Nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

3 other products · FDA event 61842

This product is part of a recall event; the main page for the event is Middle-Age Energy Booster bottles of taken orally Nokomis recalled.

ReportedClassRecallCompanyReasonWhere
CLASS IIIMiddle-Age Energy Booster bottles of taken orally Nokomis recalledMiddle-AgeH & L Jerch SalesOtherNationwide
CLASS IIIFertalin bottles of taken orally Nokomis Research Inc Bell recalledFertalinH & L Jerch SalesOtherNationwide
CLASS IIIErosyn bottles of taken orally Nokomis Research Inc Bell recalledErosynH & L Jerch SalesOtherNationwide

More recalls from H & L Jerch Sales

All 4
ReportedClassRecallCompanyReasonWhere
FoodCLASS IIIErosyn bottles of taken orally Nokomis Research Inc Bell recalledErosynH & L Jerch SalesOtherNationwide
FoodCLASS IIIFertalin bottles of taken orally Nokomis Research Inc Bell recalledFertalinH & L Jerch SalesOtherNationwide
FoodCLASS IIIMiddle-Age Energy Booster bottles of taken orally Nokomis recalledMiddle-AgeH & L Jerch SalesOtherNationwide

Other Other recalls

All 4,664