Diva Fam recalls Sea Moss Gel Superfood in four flavors over possible botulism germ contamination

The 16 oz glass jars of sea moss gel in Passion Fruit, Wildcrafted, Soursop and Mango flavors may be contaminated with Clostridium botulinum, a bacterium.

Recall details

Product

Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Passion Fruit- UPC# 5061033691882; Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Wildcrafted- UPC# 5065006235073; Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Soursop- UPC# 5061033691875

Company

Diva Fam Inc

Hazard

potential Clostridium botulinum contamination

Units

5,438,998 units across all recalled products

Where sold

Product is distributed nationwide through 31 different retail customers and direct to consumers through online sales.

FDA classification

Class II · Terminated

Classified by FDA

February 4, 2026

Recall started

January 9, 2026

FDA enforcement report

February 11, 2026

Recall closed

August 11, 2026

Identifiers

• Codes: Lot Codes: Passion Fruit- F1001, F1002, F1003, F1004, F1005, F1006, F1007, F1008, F2001, F2002
• FDA recall number: H-0472-2026
• Codes: Lot Codes: Wildcrafted- R1001, R1002, R1003, R1004, R1005, R1006, R1007, R1008, R2001, R2002, R2003, R2004, R250218, R250326, R250611
• FDA recall number: H-0469-2026
• Codes: 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
• FDA recall number: H-0478-2026
• Codes: Lot Codes: Mango- N1001, N1002, N1003, N1004, N1005, N1006, N1007, N1008, N1009, N1010, N1011, N1012, N1013, N1014, N1015, N1016, N1017, N1018, N1019, N2001, N2002, N2003, N2004, N2005, N2006, N2007, N2008, N2009, N2010, N2011, N2012, N2013, N2014, N2015, MA250104, MA250114, MA250117, MA250119, MA250131, MA250207, MA250220, MA250225, MA250305, MA250311, MA250312, MA250315, MA250318, MA250325, MA250330, MA250410, MA250413, MA250418, MA250421, MA250423, MA250430, MA250503, MA250506, MA250508, MA250512, MA250521, MA250525, MA250527, MA250608
• FDA recall number: H-0467-2026
• Codes: Lot Codes: 5 Blends in 1- G1001, G1002, G1003, G1004, G1005, G1006, G1007, G1008, G1009, G1010, G1011, G1012, G1013, G1014, G1015, G1016, G1017, G1018, G1019, G1020, G1021, G1022, G1023, G1024, G1025, G2001, G2002, G2003, G2004, G2005, G2006, G2007, G2008, G2009, G2010, G2011, G2012, G2013, G2014, G2015, G2016, G2017, G2018, ABG250102, ABG250104, ABG250119, ABG250129, ABG250218, ABG250225, ABG250227, ABG250303, ABG250305, ABG250310, ABG250313, ABG250316, ABG250319, ABG250321, ABG250407, ABG250425, ABG250501, ABG250510, ABG250512, ABG250520, ABG250522, ABG250604
• FDA recall number: H-0477-2026
• Codes: Lot Codes: Orange- O1001, O1002, O1003, O1004, O1005, O1006, O1007, O2001, O2002
• FDA recall number: H-0480-2026

The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.