FDA recall record
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Elderberry- UPC# 5065006235189
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of August 11, 2026. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Elderberry- UPC# 5065006235189
Reason
potential Clostridium botulinum contamination
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 Gel Superfood; 16 FL OZ; Glass jar sold individually. Elderberry- UPC# 5065006235189
Code information listed by FDA
Lot Codes: Elderberry- E1001, E1002, E1003, E1004, E1005, E1006, E1007, E1008, E1009, E1010, E1011, E1012, E1013, E1014, E1015, E1016, E1017, E1018, E1019, E2001, E2002, E2003, E2004, E2005, E2006, E250102, E250116, E250117, E250207, E250216, E250219, E250227, E250304, E250307, E250309, E250317, E250321, E250326, E250403, E250406, E250410, E250419, E250422, E250429, E250430, E250502, E250504, E250511, E250518, E250528, E250602, E250609, E250615
Distribution and firm information
Recalling firm listed by FDA: Diva Fam Inc
Firm location listed by FDA: San Dimas, CA, United States
Distribution reported by FDA: Product is distributed nationwide through 31 different retail customers and direct to consumers through online sales.
Product quantity listed by FDA: 5,438,998 units across all recalled products
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.