FDAFDA · Food and drugs·Recall number F-0756-2020
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
Published March 4, 2020 · Recall initiated: January 29, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
FDA sampling of senna leaves powder, an ingredient used to manufacture the Nopalina Flax Seed Fiber (powder) and Nopalina Flax Seed Fiber (capsules), tested positive for three types of Salmonella including Salmonella Gaminara, Salmonella Kentucky, and Salmonella Oranienburg.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Manufacturer
- Salud Natural Entrepreneur, Inc.
- Distributor
- Nopalina Flax Seed products are distributed throughout the United States and Puerto Rico via retail stores and the companys web site https://www.nopalinaonline.com/
- Lot
- Nopalina Flax Seed Fiber (capsules, 120 count) " Lot # 23.19 1C120#02 Best if used by 10/7/21 " Lot # 23.19.2C120#02 Best if used by 10/7/21 " Lot # 23.19.3C120#02 Best if used by 10/7/21
- Risk classification
- Class I
- Area (FDA)
- food
- Country
- United States
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