Class IIITerminated in FDA datasetMay 6, 2019

Item FG 10079, Barleans, Flax Oil, 100 Softgels per bottle.

Recalling firm: Barlean's Llc

Why it was recalled

Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

Check the codes ↓

The exact product

Item FG 10079, Barleans, Flax Oil, 100 Softgels per bottle. UPC 7 05875 1007 6. Item FG 10081, Barleans, Lignan Flax Oil, 250 Softgels per bottle. UPC 7 05875 10008 3. Item FG 70000, Barlean's, Pure Flax Oil, 45 Softgels per bottle, label in English and Bulgarian. UPC 7 05875 14004 1.

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Best By of January 2022 and earlier

TypeCode / valueContext
UPC70587510008307 6. Item FG 10081, Barleans, Lignan Flax Oil, 250 Softgels per bottle. UPC 7 05875 10008 3. Item FG 70000, Barlean's, Pure Flax Oil, 45 Softgels per bottle, label in English and Bulgarian. UPC 7 05875 14004
UPC705875140041's, Pure Flax Oil, 45 Softgels per bottle, label in English and Bulgarian. UPC 7 05875 14004 1.

Recall details

Recall number
F-1371-2019
Event ID
82565
FDA status
Terminated
Initiated
May 6, 2019
Reported
May 22, 2019
Classified
May 16, 2019
Terminated
Oct 15, 2020
Quantity
667 bottles (Item FG 10079); 1058 bottles (FG 10081); Firm did not provide for FG 7000
Location
Ferndale, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

nationwide

FDA source record · F-1371-2019

Data updated September 16, 2026. View official FDA data ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.