Nopalina Flax Seed Fiber Capsules recall: Salmonella
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
Why was Nopalina Flax Seed Fiber Capsules 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- Product
- Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
- Recalling firm
- Salud Natural Entrepreneur, Inc.
- Quantity
- 7111 bottles
- Distribution
- 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 date
- March 4, 2020
- Classification
- Class I
- Status
- Terminated
- Agency
- FDA (food)