FDA recall record
Sea Moss Tonic 16 oz and 32. oz.
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
Sea Moss Tonic 16 oz and 32. oz.
Reason
May be under-processed resulting in growth of Clostridium botulinum and lists health claims.
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.
Sea Moss Tonic 16 oz and 32. oz.
Code information listed by FDA
16 oz with upc: 196852654833 & 32 oz with upc: 196852456406 Lots: not provided
Distribution and firm information
Recalling firm listed by FDA: LIQUID BLENZ CORP
Firm location listed by FDA: Rockville Centre, NY, United States
Distribution reported by FDA: NY and online sales
Product quantity listed by FDA: 18,190 bottles total
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.