FDA recall record
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Cherry- UPC# 5061033691264
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. Cherry- UPC# 5061033691264
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. Cherry- UPC# 5061033691264
Code information listed by FDA
Lot Codes: Cherry- C1001, C1002, C1003, C1004, C1005, C1006, C1007, C1008, C1009, C1010, C1011, C1012, C2001, C2002, C2003, C250428, C250506, C250511, C250518
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.