Recalls / Class II
Class IIH-0477-2026
Product
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. 5 Blend in 1- UPC# 5061033690052
- Type
- Food
- Affected lot / code info
- 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
- Quantity
- 5,438,998 units across all recalled products
Why it was recalled
potential Clostridium botulinum contamination
Recalling firm
- Firm
- Diva Fam Inc
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 210 W Arrow Hwy Ste E, N/A, San Dimas, California 91773-3360
Distribution
- Distribution pattern
- Product is distributed nationwide through 31 different retail customers and direct to consumers through online sales.
Timeline
- Recall initiated
- 2026-01-09
- FDA classified
- 2026-02-04
- Posted by FDA
- 2026-02-11
- Status
- Ongoing
Source: openFDA Food Enforcement endpoint. Recall record H-0477-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings.