FDA recall record
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Blue Spirulina and Raspberry- UPC# 5065006235813
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. Blue Spirulina and Raspberry- UPC# 5065006235813
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. Blue Spirulina and Raspberry- UPC# 5065006235813
Code information listed by FDA
Lot Codes: Blue Spirulina and Raspberry- B1001, B1002, B1003, B1004, B1005, B1006, B1007, B1008, B1009, B1010, B1011, B1012, B1013, B1014, B1015, B1016, B1017, B1018, B2001, B2002, B2003, B2004, B2005, B2006, B2007, SPB241229, SPB250104, SPB250119, SPB250124, SPB250207, SPB250219, SPB250225, SPB250301, SPB250306, SPB250310, SPB250318, SPB250323, SPB250404, SPB250429, SPB250502, SPB250506, SPB250514, SPB250520, SPB250521
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.