Recall record at a glance
| Official record | F-0756-2020 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Salud Natural Entrepreneur, Inc. |
| Report date | Mar 4, 2020 |
| Recall initiation date | Jan 29, 2020 |
| Quantity | 7111 bottles |
| Location | Waukegan, IL, United States |
Official product description
Nopalina Flax Seed Fiber Capsules, 120 count bottle, UPC 8 90523 00086 7
Why the product 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.
Distribution information
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/
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Press Release.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
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