RECALL DATABASE

Sea Moss Gel Recall: Diva Fam Passion Fruit

Announced 2026-02-11 · FDA

The recall affects Diva Fam Inc Sea Moss Gel Superfood, 16 fl oz glass jar in the Passion Fruit flavor, distributed nationwide through 31 retailers and online sales. The recall is due to potential Clostridium botulinum contamination. No corrective action is listed in the provided information.

BrandDiva Fam Inc
ProductSea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Blue Spirulina and Raspberry- UPC# 5065006235813
Reasonpotential Clostridium botulinum contamination
Severitymoderate
Units affected5438998
DistributionProduct is distributed nationwide through 31 different retail customers and direct to consumers through online sales.
AgencyFDA

WHAT YOU SHOULD DO

  1. Stop using the product and discard any remaining jars.
  2. Check for the Passion Fruit flavor and 16 oz glass jar; contact the retailer or Diva Fam customer service for disposal or refund instructions.
  3. Monitor for botulism symptoms and seek medical care if symptoms occur.

How to identify the recalled item

Lot / date codesLot Codes: Blue Spirulina and Raspberry- B1001, B1002, B1003, B1004, B1005, B1006, B1007, B1008, B1009, B1010, B1011, B1012, B1013, B1014, B1015, B1016, B1017, B1018, B2001, B2002, B2003, B2004, B2005, B2006, B2007, SPB241229, SPB250104, SPB250119, SPB250124, SPB250207, SPB250219, SPB250225, SPB250301, SPB250306, SPB250310, SPB250318, SPB250323, SPB250404, SPB250429, SPB250502, SPB250506, SPB250514, SPB250520, SPB250521
Lot / date codesLot Codes: Passion Fruit- F1001, F1002, F1003, F1004, F1005, F1006, F1007, F1008, F2001, F2002

These are the identifiers FDA published for this recall. Most recall notices list no UPC or model number at all — if the code on your item is not shown here, that does not mean the item is excluded. Check the official notice, or contact the company.

This is an automatically maintained record of an official recall notice. Details can change; always follow the official notice linked above. See all records in the Recall Database.