Food Recall Check
Class III · Low risk Terminated Initiated May 6, 2019 (7 years ago)

Item FG 10089 Barlean s recall

Recalled by Barlean's Llc · Ferndale, WA, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

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.

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

Item 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.

Quantity: 1845 bottles (FG 10089); 3606 bottles (FG 10090)

Food: Seafood & fish Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Best By of January 2022 and earlier

Where it was sold

Nationwide.

FDA's distribution note: nationwide

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Barlean's Llc
Initiated by
Voluntary: Firm initiated
Recall initiated
May 6, 2019
In FDA report of
May 22, 2019
Terminated
Oct 15, 2020
FDA recall number
F-1363-2019 · event 82565
Official record
FDA enforcement report search

Also recalled with it (11 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class III · Low risk Terminated Labeling

Item FG 10083 Barlean's

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

Barlean's Llc Nationwide F-1360-2019
Class III · Low risk Terminated Labeling

Item FG 10084 Barlean s

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

Barlean's Llc Nationwide F-1361-2019
Class III · Low risk Terminated Labeling

Item FG 10085 Barleans

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

Barlean's Llc Nationwide F-1362-2019
Class III · Low risk Terminated Labeling

Item FG 10106 Barlean s

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

Barlean's Llc Nationwide F-1364-2019
Class III · Low risk Terminated Labeling

Item FG 10116 Barlean s

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

Barlean's Llc Nationwide F-1365-2019
Class III · Low risk Terminated Labeling

Item FG 10146 Barlean s

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

Barlean's Llc Nationwide F-1366-2019
Class III · Low risk Terminated Labeling

Item FG 10149 Barlean s

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

Barlean's Llc Nationwide F-1367-2019
Class III · Low risk Terminated Labeling

Item FG 10079 Barleans

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

Barlean's Llc Nationwide F-1371-2019