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Class III: unlikely to cause harmTerminated

H & L Jerch Sales Fertalin bottles of 90 tablets taken orally Recall

Fertalin bottles of 90 tablets taken orally Nokomis Research Inc Bell Lifestyle Produc…

H & L Jerch Sales, Inc. · South Haven, MI

Risk level
Class III
Reported by FDA
Jul 18, 2012
Recall ID
F-1731-2012
Check your lot numberHow we source this data

Summary

H & L Jerch Sales recalled Fertalin bottles of 90 tablets taken orally starting Jun 11, 2012. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-1731-2012 on Jul 18, 2012. Reason: 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. Status: Terminated.

Why it was 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.

Product description

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

Lot numbers, UPCs & expiration codes

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

Where it was sold

Nationwide

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1731-2012
Classification
Class III
Status
Terminated
Recall initiated
Jun 11, 2012
FDA report date
Jul 18, 2012
Quantity
688 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
H & L Jerch Sales, Inc.

Original FDA data

Every field from FDA enforcement report F-1731-2012, exactly as published.

Show all FDA fields
City
South Haven
State
MI
Status
Terminated
Country
United States
Event ID
61842
Address
07090 68th St
Code information
Catalog number: #8: UPC 771733109024; and lot numbers: 11157, 12103, 12221, and 12289.
Postal code
49090-8119
Report date
Jul 18, 2012
Product type
Food
Recall number
F-1731-2012
Classification
Class III
Recalling firm
H & L Jerch Sales, Inc.
Product quantity
688 bottles
Termination date
Feb 12, 2013
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Fertalin bottles of 90 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #8
Distribution pattern
Nationwide
Recall initiation date
Jun 11, 2012
Initial firm notification
Letter
Center classification date
Jul 6, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1731-2012, published Jul 18, 2012. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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