Item 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 LLC recalled Item FG 10146, Barlean s, Essential Woman, 120 count Softgels per bottle in a Class III action, the FDA tier used when a product is unlikely to cause adverse health effects, typically for labeling or minor regulatory issues on May 6, 2019.

The FDA listed the reason as an undeclared allergen: "Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm." Allergen mislabeling is the leading cause of U.S. food recalls, because a missing declaration can trigger a reaction in someone who reads the label and believes the product is safe.

Distribution was broad: the FDA record describes it as "nationwide," which places this among the wider-reach recalls on the site. Consumers across the affected area should check product on hand. The recalling firm is based in Ferndale, WA. The recall covers 1144 bottles (FG 10146) and 1913 bottles (FG 10147) of product. The FDA has Terminated this recall (first reported May 22, 2019), its final lifecycle state, indicating the agency considers the corrective action resolved. The historical record remains useful for tracking a brand's recall pattern over time.