Severity
Low
LowClass IIITerminated
FDA Food recall · Reported July 18, 2012
Erosyn bottles of 30 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #7
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…
Compiled from official public sources by the editorial team.
Verify with FDA Food →
H & L Jerch Sales, Inc. recalled Erosyn bottles of 30 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #7 - a low-severity action.
Erosyn bottles of 30 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #7 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-1730-2012 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-1730-2012 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1730-2012) 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 8260 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, 1 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.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,049 drugs & medications recalls on record
Where this recall sits in the database
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. 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
8260 bottles
Related Recalls
6
1 from same agency
Product description
Erosyn bottles of 30 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #7
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-1730-2012 |
| Date reported | July 18, 2012 |
| Date initiated | June 11, 2012 |
| Recalling firm | H & L Jerch Sales, Inc. |
| Firm location | South Haven, MI |
| Affected scope | 8260 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-1730-2012) 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? ▼
Erosyn bottles of 30 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #7. Recalled by H & L Jerch Sales, Inc.. Units affected: 8260 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-1730-2012.
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-1730-2012) 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.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported July 18, 2012.
- Source: FDA - Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC - Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA - National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. 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 July 2026.