Class IITerminatedVoluntary: Firm initiated
Bioriginal Food & Science Corporation: food recall F-0709-2025
Bioriginal Food & Science Corporation of Saskatoon recalled Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil 16 Fl oz / 473 ml, Dietary Supplement, Black HDPE plastic bottle with… Reason: Undeclared allergens: Soy lecithin. The FDA listed it as Class II in its Enforcement Report dated Apr 9, 2025; distribution: Puerto Rico.
Record status as published: Terminated (terminated Sep 3, 2025). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil 16 Fl oz / 473 ml, Dietary Supplement, Black HDPE plastic bottle with cap, Manufactured for Natural Slim, San Juan Puerto Rico
- Product quantity
- 61 bottles
- Reason for recall
- Undeclared allergens: Soy lecithin
- Codes, lots and dates on the package
- Lot Code: PRP403337
- Distribution pattern
- Puerto Rico
- Recalling firm
- Bioriginal Food & Science Corporation, Saskatoon, Canada
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Mar 21, 2025 |
| Classified by the FDA | Apr 14, 2025 |
| Published in the Enforcement Report | Apr 9, 2025 |
| Terminated | Sep 3, 2025 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number F-0709-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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