Nationwide Sea Moss Gel Recall Issued Over Risk of Foodborne Illness

A Los Angeles-based company has announced a voluntary recall of its popular sea moss gel products distributed across the country, citing potential contamination risks tied to a rare but serious foodborne illness.

Diva Fam Inc. initiated the recall of all batches of its True Sea Moss brand Sea Moss Gel Superfood on Jan. 9, according to an FDA announcement published Monday. The affected products are packaged in 16-fluid-ounce glass jars and were distributed nationwide through retail outlets and online channels.

The company pulled the products from shelves after a California Department of Public Health inspection found deficiencies in the company’s regulatory authorization and temperature monitoring for pH-controlled food products. Products lacking proper manufacturing oversight create conditions where dangerous microorganisms could potentially develop, potentially creating conditions for organisms that can produce toxins associated with Botulism.

The rare but serious illness can affect the nervous system. Symptoms may include general weakness, dizziness, double vision, difficulty speaking or swallowing, and in severe cases, difficulty breathing or muscle weakness.

The recalled gel came in 11 flavors, each with distinct product codes. True Sea Moss brand Sea Moss Gel Superfood was available in Mango, Pineapple, Wildcrafted, Apple and Cinnamon, Elderberry, Passion Fruit, Blue Spirulina and Raspberry, Strawberry, Cherry, Mango and Pineapple, 5 Blends in 1, Soursop, Lemon Pie and Orange varieties.

Consumers can identify affected products by checking the manufacture date, indicated on the jar lid in MM/YYYY format. All products manufactured before Jan. 9 fall under the recall notice.

Despite the potential health risk, no illnesses or adverse reactions have been reported in connection with the recalled products to date.

The red algae, also known as Irish moss or Chondrus crispus, grows in shallow coastal waters worldwide. Historically, it served as a nutritional source during Ireland's 19th-century Potato Famine.

Symptoms progress from initial neurological effects to potentially severe complications. Mayo Clinic notes that severe cases can result in paralysis and breathing difficulties.

Consumers who purchased affected products should discontinue use immediately and contact their retailer regarding return or disposal options. The FDA is overseeing the recall process.