FDA recall record

Barlean's Item FG 10084, Barlean s, Ultra EPA Fish Oil 1250 mg Omega-3 recall — FDA F-1361-2019

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

Class IIIclassification
F-1361-2019official record ID
May 22, 2019report date

Recall record at a glance

Official recordF-1361-2019
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBarlean's LLC
Report dateMay 22, 2019
Recall initiation dateMay 6, 2019
Quantity32 bottles
LocationFerndale, WA, United States

Official product description

Item FG 10084, Barlean s, Ultra EPA Fish Oil 1250 mg Omega-3, 60 softgels per bottle, UPC 7 05875 61005 6.

Why the product was recalled

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

Distribution information

nationwide

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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