Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement,

NatureAll-Stf Holding, LLC recalled Acidophilus-Plus, No. 102, 90 Capsules, Dietary Supplement in a Class I action — the FDA's most serious tier, reserved for products with a reasonable probability of causing serious health consequences or death on Jul 26, 2017.

The FDA listed the reason as an undeclared allergen: "Undeclared allergens: milk (Colostrum, Dried Yogurt, Whey)." 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, US: CA, FL, GA, ID, IL, IN, TX, UT, WA, WY. No foreign or govt/VA/military consignees," 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 Salt Lake City, UT. The recall covers 367 bottles of product. The FDA has Terminated this recall (first reported Aug 23, 2017), 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.