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Class III: unlikely to cause harmTerminated

H & L Jerch Sales Product Name: Eroxil bottles of 30 tablets Recall

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

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

Risk level
Class III
Reported by FDA
Jul 18, 2012
Recall ID
F-1729-2012
Check your lot numberHow we source this data

Summary

H & L Jerch Sales recalled Product Name: Eroxil bottles of 30 tablets starting Jun 11, 2012. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report F-1729-2012 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

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

Lot numbers, UPCs & expiration codes

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

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-1729-2012
Classification
Class III
Status
Terminated
Recall initiated
Jun 11, 2012
FDA report date
Jul 18, 2012
Quantity
50,604 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
H & L Jerch Sales, Inc.

Original FDA data

Every field from FDA enforcement report F-1729-2012, 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: #6: UPC 771733109000; and lot numbers: 11154, 11185, 11186, 11267, 11269, 12014, 12057, 12099, 12220, and 12244.
Postal code
49090-8119
Report date
Jul 18, 2012
Product type
Food
Recall number
F-1729-2012
Classification
Class III
Recalling firm
H & L Jerch Sales, Inc.
Product quantity
50,604 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
Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6
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-1729-2012, published Jul 18, 2012. View the source record (openFDA) · FDA enforcement reports

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

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