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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 61842

4 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
June 11, 2012
Product types
Food
Classifications
Class III
Statuses
Terminated
Recalling firm wording
H & L Jerch Sales, Inc.

Dossier provenance

Source snapshots represented here

  • openFDA Food Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

4 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

food · product 1 of 4

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

F-1729-2012
Recall number
F-1729-2012
Initiated
June 11, 2012
Classification
Class III
Status
Terminated
Recalling firm
H & L Jerch Sales, Inc.
Quantity
50,604 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

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

Distribution pattern

Nationwide

food · product 2 of 4

Erosyn bottles of 30 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #7

F-1730-2012
Recall number
F-1730-2012
Initiated
June 11, 2012
Classification
Class III
Status
Terminated
Recalling firm
H & L Jerch Sales, Inc.
Quantity
8260 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Catalog number: #7: UPC 771733109017; and lot numbers: 11155, 11190, and 12102.

Distribution pattern

Nationwide

food · product 3 of 4

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

F-1731-2012
Recall number
F-1731-2012
Initiated
June 11, 2012
Classification
Class III
Status
Terminated
Recalling firm
H & L Jerch Sales, Inc.
Quantity
688 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Catalog number: #8: UPC 771733109024; and lot numbers: 11157, 12103, 12221, and 12289.

Distribution pattern

Nationwide

food · product 4 of 4

Middle-Age Energy Booster bottles of 60 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #65

F-1732-2012
Recall number
F-1732-2012
Initiated
June 11, 2012
Classification
Class III
Status
Terminated
Recalling firm
H & L Jerch Sales, Inc.
Quantity
1981 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
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.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

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.

Code information

Catalog number: #65: UPC 771733110372; and lot numbers: 11156,12104, 12222, and 12290.

Distribution pattern

Nationwide