Barlean's Llc FDA recall records

The FDA has published 12 food recall enforcement records naming Barlean's Llc between 2019 and 2019, covering 1 separate recall events. The firm is recorded in Washington. Data last updated 2 September 2026.

Records of 29,386
12
Share of all recalls
0%
Class I of 12
0
Reported between
2019 to 2019

What these records are

Every record on this page was published by the FDA in the openFDA food enforcement database. 12 records cover 1 recall events, because the agency opens one record per product code: a single recall of a product line with many codes appears here many times.

0 of these records are Class I, 0 Class II and 12 Class III. A recall count is not a safety score. Most FDA food recalls are initiated by the firm itself, and a recall is the firm removing product from the market, which is what a food safety plan is built to produce.

What was recalled for

A single record can name more than one hazard, so these counts overlap.

By year

Counts are by the date the FDA reported the enforcement action. That date runs behind the date a firm started a recall, so the most recent year is always partial.

Where the recalling firms are

The state is the location of the recalling firm, not where the product was sold. Distribution is recorded separately on each record.

Most recently reported

All 12 records.
ReportedProductFirmReasonClass
2019-05-22Item 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.Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10146, Barlean s, Essential Woman, 120 count Softgels per bottle, UPC 7 05875 10013 7. Item FG 10147, Barlean s, Essential Woman, 60 count Softgels per bottle, UPC 7 05875 10009 0.Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10084, Barlean s, Ultra EPA Fish Oil 1250 mg Omega-3, 60 softgels per bottle, UPC 7 05875 61005 6.Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10083, Barlean's, Ultra DHA Fish Oil Omega-3, Lemonade Flavor, 90 softgels per bottle, UPC 7 05875 61004 9.Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10037, Barlean s Cod Liver Oil Omega 3 EPA/DHA with Added Vitamin D, 100 softgel per bottle. UPC 7 05875 61010 0Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle, UPC 7 05875 10019 9Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10085, Barleans, Ultra EPA-DHA Fish Oil 1,300 mg Omega-3 Orange Flavor, 60 Softgels per bottle. UPC 7 05875 61006 3.Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10106, Barlean s, Olive Leaf Complex, 120 Softgels per bottle. UPC 7 05875 70009 2. Item FG 10107, Barlean s, Olive Leaf Complex, 60 Softgels per bottle. UPC 7 05875 0008 5.Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10190, Barleans Full Spectrum Hemp Extract, 60 Softgels per bottle. UPC 7 05875 80113 3. Item FG 10193, Barleans Full Spectrum Hemp Extract, 30 Softgels per bottle. UPC 7 05875 80115 7.Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10089, Barlean s, Fish Oil Omega-3 EPA/DHA Orange Flavor, 100 Softgels per bottle. UPC 7 05875 61007 0. Item FG 10090, Barlean s, Fish Oil Omega-3 EPA/DHA Orange Flavor, 250 Softgels per bottle. UPC 7 05875 61008 7.Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10191, Barlean s Ideal CBD Hemp Oil Softgel, 900 mg CBD, Less than 0.3% THC, 60 Softgels per bottle. UPC 7 05875 80112 6. Item FG 10194, Barlean s Ideal CBD Hemp Oil softgel, 750 mg CBD, Less than 0.3% THC, 30 Softgels per bottle. UPC 7 05875 80114 0.Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III
2019-05-22Item FG 10116, Barlean s, Master Blend Total Omega 3.6.9 Lemonade Flavor, 90 Softgels per bottle. UPC 7 05875 10020 5.Barlean's LlcBarlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.Class III

Questions

How many FDA recalls has Barlean's Llc had?
The FDA has published 12 food recall enforcement records naming Barlean's Llc between 2019 and 2019. Those records cover 1 separate recall events: the agency opens one record per product code, so one recall of a product line appears as many records.
Does a high recall count mean a firm is unsafe?
Not on its own. Most FDA food recalls are initiated voluntarily by the firm, and a recall is the firm removing product from the market, which is what a working food safety plan is supposed to produce. Record counts also scale with the number of product codes a firm carries rather than with the number of things that went wrong.

All FDA food recall data

A recall is the end of an evidence trail that either existed or did not. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.