Severity
Low
LowClass IIITerminated
FDA Food recall · Reported July 18, 2012
Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6
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 cons…
H & L Jerch Sales, Inc. recalled Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6 - a low-severity action.
Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6 was recalled by H & L Jerch Sales, Inc. in July 18, 2012. Reason: The products contain synthetic equivalents of spermine and/or spermidine, which are constituents or extracts …. Check the official notice for the remedy. Verify recall #F-1729-2012 with the FDA Food before acting.
The recall
H & L Jerch Sales, Inc. issued this low-severity FDA Food recall-The products contain synthetic equivalents of spermine and/or spermidine, which are constituents or extracts ….
- Low
- severity level
- Class III
- classification
- July 18, 2012
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1729-2012 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1729-2012) was formally reported on July 18, 2012, with the manufacturer initiating the action on June 11, 2012. It is classified under Low severity (Class III), with a current status of Terminated. H & L Jerch Sales, Inc. is listed as the recalling firm, operating out of South Haven, MI. Federal records list the affected scope as 50,604 bottles.
The documented reason for this recall is: 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 b… Distribution data in the federal record shows the product reached: Nationwide. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,012 dietary supplements recalls on record
Of 88,001 recalls with an agency hazard classification, 19,020 are high severity, 64,468 moderate, and 4,513 low. A further 16,157 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
50,604 bottles
Related Recalls
6
6 from same agency
Product description
Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-1729-2012 |
| Date reported | July 18, 2012 |
| Date initiated | June 11, 2012 |
| Recalling firm | H & L Jerch Sales, Inc. |
| Firm location | South Haven, MI |
| Affected scope | 50,604 bottles |
| Distribution | Nationwide |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1729-2012) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6. Recalled by H & L Jerch Sales, Inc.. Units affected: 50,604 bottles.
Why was this product 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 agency issued this recall? ▼
This recall was issued by the FDA Food on July 18, 2012. Severity: Low. Recall number: F-1729-2012.
Where was the recalled product distributed? ▼
Distribution: Nationwide.
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1729-2012) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nationwide recalls with similar severity or category timing
Two federal-filing-derived peer sets for this notice, both outside the same recalling firm and filing state so the neighborhoods are not firm or geographic containment.
Similar severity · nearest report date
Same archive severity grade (Low), closest by report date among other firms and states.
Similar Dietary Supplements · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
Showing 5 of 2015 other recalls in this category.
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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported July 18, 2012. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.