Bacaolinita Liquid Dietary Supplement With vitamins A and D + B12 8 fl. oz (236 mL) UPC 841548000028 packaged in a bottle inside a cardboard box

Procaps S.a. de C.v. recalled Bacaolinita Liquid Dietary Supplement With vitamins A and D + B12 8 fl. oz (236 mL) UPC 841548000028 packaged in a bottle inside a cardboard in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on May 19, 2023.

The FDA listed the reason as an undeclared allergen: "PEG-40 not declared as an ingredient on the label" 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.

The product reached multiple states, recorded by the FDA as "DE, TX, CA." A multi-state footprint means the same lot can surface in households far from the producer. The recalling firm is based in Soyapango. The recall covers 33,684 Boxes of product. The FDA has Terminated this recall (first reported Jun 14, 2023), 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.