FDA Recalls Middle-Age Energy Booster Tablets Due to Unapproved Ingredients
H & L Jerch Sales, Inc. is recalling 1,981 bottles of Middle-Age Energy Booster tablets nationwide because they contain unapproved synthetic botanical ingredients.
What this means for you
Cosmetic or documentation issue. No expected health impact, but the manufacturer is correcting the affected products.
Our severity reasoning: The FDA classified this as a Class III recall, which indicates the product is unlikely to cause adverse health consequences. The issue is regulatory (unapproved ingredients) rather than a direct safety hazard like contamination or injury.
Plain-English summary
H & L Jerch Sales, Inc. is recalling 1,981 bottles of Middle-Age Energy Booster tablets, manufactured by Nokomis Research Inc and sold under the Bell Lifestyle Products brand. The product is distributed nationwide and includes catalog number #65, UPC 771733110372, and lot numbers 11156, 12104, 12222, and 12290.
The recall was initiated because the tablets contain synthetic equivalents of spermine and/or spermidine. The FDA determined that synthetic copies of constituents or extracts of herbs or other botanicals are not considered dietary ingredients and must be approved for use in dietary supplements. The use of these specific ingredients has not been approved.
Consumers who have purchased these products should stop using them and return them to the place of purchase for a refund or contact the recalling firm for further instructions.
The recalled product
- Product
- Middle-Age Energy Booster bottles of 60 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #65
- Manufacturer
- H & L Jerch Sales, Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 1,981
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (5)
- Catalog number: #65: UPC 771733110372
- and lot numbers: 11156
- 12104
- 12222
- and 12290.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 4 recalled by H & L Jerch Sales, Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 4 products in this recall →Related recalls
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