Diva Fam Inc Issues Nationwide Recall of Sea Moss Gel Superfood Over Botulism Concerns

Source: FDA · United States

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Diva Fam Inc has voluntarily recalled over 5.4 million units of Passion Fruit Sea Moss Gel Superfood due to potential contamination with Clostridium botulinum.

What this FDA recall tells you, and what most readers miss

This notice was issued by FDA on April 6, 2026 and geographically references United States. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.

Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.

Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, food.

What Happened

Diva Fam Inc, based in San Dimas, California, has initiated a voluntary recall of its Sea Moss Gel Superfood products. The recall was prompted by the potential contamination of the product with Clostridium botulinum. The FDA has classified this as a Class II recall, which is currently ongoing.

Which Products Are Affected

The recall specifically affects the Passion Fruit flavor of the Sea Moss Gel Superfood. The product details are as follows:

  • Product Name: Sea Moss Gel Superfood (Passion Fruit)
  • Packaging: 16 FL OZ glass jars, sold individually
  • UPC: 5061033691882
  • Lot Codes: F1001, F1002, F1003, F1004, F1005, F1006, F1007, F1008, F2001, and F2002
  • Quantity: 5,438,998 units are affected across all recalled products.

These products were distributed nationwide through 31 different retail customers and sold directly to consumers via online sales.

What You Should Do

Consumers who have purchased the affected Passion Fruit Sea Moss Gel Superfood should immediately stop using the product. The recall was initiated on January 9, 2026, and notification was conducted through various channels including email, fax, letter, and press releases. Consumers may contact Diva Fam Inc at their San Dimas, CA location for further information regarding the recall.

Why This Matters

Potential contamination with Clostridium botulinum poses a significant health risk, as the bacteria can produce life-threatening toxins that cause botulism, a serious form of food poisoning.

Source

Information provided by the FDA under recall number H-0472-2026.

Original source: FDA Official Notice ↗

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Frequently Asked Questions

Common questions about this FDA recall.

What is this FDA recall about?
Diva Fam Inc has voluntarily recalled over 5.4 million units of Passion Fruit Sea Moss Gel Superfood due to potential contamination with Clostridium botulinum.
Which agency issued this alert?
This alert was issued by FDA. The original notice is available at the source link at the bottom of this article.
How severe is this alert?
This alert is classified as "high" severity. Take precautions and monitor for updates.
What area is affected?
This alert affects United States. Check with FDA for the most current geographic scope.
Where can I find more FDA Recalls updates?
Browse the full FDA Recalls feed on Areazine at areazine.com/recalls/fda/ for the latest updates from FDA and other agencies.