Addback Tablet Dietary Supplement 60 tablets per 190cc Oblong WHDPE bottle Net Wet: 85gm (60 tablet wt) UPC- 0651536124526 Firm name Prevent D Labs Division of CAYS, LLC Southington, CT

Cays LLC recalled Addback Tablet in a Class II action, the FDA tier for products that may cause temporary or medically reversible health effects on Mar 29, 2019.

The FDA listed the reason as an undeclared allergen: "Undeclared coating ingredients: HPMC, Triacetin, Titanium Dioxide, FD & C Yellow # 5, FD & C Yellow # 6, FD & C Blue # 1. In addition, the label states Silicon Dioxide, which is not part of the formulation" 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 limited; the FDA record lists "All product is in the firm's possession." Single-area recalls still warrant a kitchen check for anyone who shops within that footprint. The recalling firm is based in Southington, CT. The recall covers 2095 bottles of product. The FDA has Terminated this recall (first reported Apr 24, 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.