Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil 16 Fl oz / 473 ml, Dietary Supplement, Black HDPE plastic bottle with ca
Summary
The FDA issued a Class II for Fresh Flax Oil OMEGA 3-6-9 Organic Flaxseed Oil 16 Fl oz / 473 ml, Dietary Suppl by Bioriginal Food & Science Corporation. Reason: Undeclared allergens: Soy lecithin.
Details
Source
Food Recall
External ID
F-0709-2025
Action Date
2025-04-09
Status
Terminated
Category
food
Product Description
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
Lot/Code Info: Lot Code: PRP403337
Quantity Affected: 61 bottles
Reason for Recall
Undeclared allergens: Soy lecithin
Distribution
Puerto Rico
Type: Voluntary: Firm initiated
Recall Initiated: 2025-03-21
Company
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 32 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Bioriginal Food & Science Corporation) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Bioriginal Food & Science Corporation have FDA actions?
This is the only FDA action we have on record for Bioriginal Food & Science Corporation in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0709-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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