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RECALL RECORD — CLASS IIIRecall closedF-1731-2012/FDA enforcement
H & L Jerch Sales, INC.·Food·Jun 11, 2012

Fertalin Bottles of 90 Tablets Taken Orally Nokomis Research INC Bell Lifestyle Products #8

What you need to know

Class III

  • What happened

    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…

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDANationwide (US)More food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameH & L Jerch Sales, INC.
Recalling firmH & L Jerch Sales, INC.South Haven, MI, United States
UPC / barcodes
7 71733 10902 4
Lot / date codes
  • Catalog number: #8: UPC 771733109024
  • and lot numbers: 11157, 12103, 12221, and 12289.
Distribution area
Nationwide

Nationwide

United States

Quantity affected688 bottles
Recall initiationFDA report date: July 18, 2012
FDA recall numberF-1731-2012

Beyond the headline

The recall, in context

H & L Jerch Sales, INC. initiated this food recall on June 11, 2012. The FDA enforcement report states: 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. The FDA report lists distribution as: Nationwide.

The FDA enforcement report describes the reason as: 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.

Fertalin Bottles of 90 Tablets Taken Orally Nokomis Research INC Bell Lifestyle Products #8 was made or distributed by H & L Jerch Sales, INC. in South Haven, MI, United States. This page reflects FDA report F-1731-2012, dated July 18, 2012.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Fertalin Bottles of 90 Tablets Taken Orally Nokomis Research INC Bell Lifestyle Products #8 recall?

H & L Jerch Sales, INC. recalled Fertalin Bottles of 90 Tablets Taken Orally Nokomis Research INC Bell Lifestyle Products #8 in an FDA Class III enforcement action reported as F-1731-2012. 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…

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the H & L Jerch Sales, INC. recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-1731-2012. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.