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FDA recall record

ELV Control Herbal Supplement; 90 Capsules

Recall F-1391-2024Class IOngoingApril 3, 2024

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

Product described in an FDA recall

ELV Control Herbal Supplement; 90 Capsules

Reason

FDA Analysis found product labeled as tejocote is actually yellow oleander, which is toxic to humans.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • ELV Control Herbal Supplement; 90 Capsules

Code information listed by FDA

N1082701 050328; GESPM240622 071324; GESPM300; 622 071324; GESPM050722 071324; 190620230009B 061928; 190620231573678B 062828280620231; 573678BA 062828

Distribution and firm information

Recalling firm listed by FDA: World Green Nutrition Inc.

Firm location listed by FDA: San Antonio, TX, United States

Distribution reported by FDA: Product is sold through authorized dealers and E-commerce throughout the USA and Mexico, While the products, Elv Control Herbal Supplement and Mexican Tejocote Root Supplement Pieces (Raiz de Tejocote Mexicano Suplemento en Trozos), were intended to be distributed only through authorized distributors, it is possible that these products were purchased and further distributed via e-commerce platforms and/ or physical stores.

Product quantity listed by FDA: 20,092 units

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.