Middle-Age Energy Booster (H & L Jerch) – Botanical Ingredient Concerns (2012)
Class III: A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences
Class III recall indicates unlikely adverse health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Middle-Age Energy Booster bottles of 60 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #65
Brand
H & L Jerch Sales, Inc.
Lot Codes / Batch Numbers
Catalog number: #65: UPC 771733110372, and lot numbers: 11156, 12104, 12222, and 12290.
Products Sold
Catalog number: #65: UPC 771733110372; and lot numbers: 11156,12104, 12222, and 12290.
H & L Jerch Sales, Inc. is recalling Middle-Age Energy Booster bottles of 60 tablets taken orally Nokomis Research Inc Bell Lifestyle Pr due to The products contain synthetic equivalents of spermine and/or spermidine, which are constituents or extracts of an herb or other botanical, and the th. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026