Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Wildcrafted- UPC# 5065006235073
Summary
The FDA issued a Class II for Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Wildcrafted- UPC# by Diva Fam Inc. Reason: potential Clostridium botulinum contamination.
Details
Source
Food Recall
External ID
H-0469-2026
Action Date
2026-02-11
Status
Ongoing
Category
food
Product Description
Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Wildcrafted- UPC# 5065006235073
Lot/Code Info: Lot Codes: Wildcrafted- R1001, R1002, R1003, R1004, R1005, R1006, R1007, R1008, R2001, R2002, R2003, R2004, R250218, R250326, R250611
Quantity Affected: 5,438,998 units across all recalled products
Reason for Recall
potential Clostridium botulinum contamination
Distribution
Product is distributed nationwide through 31 different retail customers and direct to consumers through online sales.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-01-09
Company
San Dimas, CA
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 69 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Diva Fam Inc has 14 FDA actions in our database, including 14 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Diva Fam Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Diva Fam Inc have FDA actions?
Diva Fam Inc has 14 FDA actions in our database, including 14 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0469-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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