FDA recall record
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Soursop- UPC# 5061033691875
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. Soursop- UPC# 5061033691875
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. Soursop- UPC# 5061033691875
Code information listed by FDA
Lot Codes: Soursop- Q1001, Q1002, Q1003, Q1004, Q1005, Q1006, Q1007, Q1008, Q1009, Q1010, Q1011, Q1012, Q1013, Q1014, Q1015, Q1016, Q1017, Q1018, Q2001, Q2002, Q2003, Q2004, Q2005, Q2006
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.