Why it was recalled
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.
Product description
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
Lot numbers, UPCs & expiration codes
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
Where it was sold
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/
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-0756-2020
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- Jan 29, 2020
- FDA report date
- Mar 4, 2020
- Quantity
- 7111 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Salud Natural Entrepreneur, Inc.
Original FDA data
Every field from FDA enforcement report F-0756-2020, exactly as published.
Show all FDA fields
- City
- Waukegan
- State
- IL
- Status
- Terminated
- Country
- United States
- Event ID
- 84812
- Address
- 1120 Glen Rock Ave
- Code information
- 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
- Postal code
- 60085-5458
- Report date
- Mar 4, 2020
- Product type
- Food
- Recall number
- F-0756-2020
- Classification
- Class I
- Recalling firm
- Salud Natural Entrepreneur, Inc.
- Product quantity
- 7111 bottles
- Termination date
- Nov 3, 2020
- Reason for recall
- 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.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
- Distribution pattern
- 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/
- Recall initiation date
- Jan 29, 2020
- Initial firm notification
- Press Release
- Center classification date
- Feb 26, 2020