Published by If you purchased True Sea Moss Sea Moss Gel Superfood that has been recalled for a potential botulism-related health risk and you became ill or incurred related expenses, you may qualify for a free legal review.
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Table Of Contents
What’s the Problem?
On January 9, 2026, Diva Fam Inc. announced a voluntary recall of all lots and flavors of True Sea Moss brand Sea Moss Gel Superfood due to a lack of required regulatory authorization and temperature monitoring records for pH-controlled food products. pH-controlled foods that are not manufactured in line with applicable requirements may present a risk of microbial growth, including organisms that can produce toxins associated with botulism. Botulism is a rare but serious illness affecting the nervous system, with symptoms that can include weakness, dizziness, double vision, difficulty speaking or swallowing, and in severe cases, difficulty breathing or muscle weakness.
As of the recall announcement, no illnesses or adverse health events had been reported in connection with the recalled products. The recall applies to Sea Moss Gel Superfood packaged in 16 FL OZ (473 mL) glass jars manufactured prior to January 9, 2026, with the manufacture date (MFD) indicated on the can lid in MM/YYYY format.
Latest Updates
- January 9, 2026 – Diva Fam Inc. announced a voluntary recall of all lots and flavors of True Sea Moss Sea Moss Gel Superfood due to missing regulatory authorization and temperature monitoring records for pH-controlled food products, creating a potential botulism-related health risk. [1]
- January 12, 2026 – FDA published the company’s recall announcement and identified the recall reason category as “Potential Foodborne Illness – Botulism” for True Sea Moss Sea Moss Gel Superfood in various flavors (16 FL OZ glass jars). [1]
- January 12, 2026 – The recall notice listed affected flavors and UPCs and directed consumers to discontinue use and follow return or disposal instructions from the place of purchase. [1]
Product & Usage Overview
The recall covers True Sea Moss brand Sea Moss Gel Superfood packaged in 16 FL OZ (473 mL) glass jars, across all lots and flavors, manufactured prior to January 9, 2026. The manufacture date (MFD) appears on the can lid in MM/YYYY format, which can help consumers identify recalled products still in their homes.
FDA’s posted announcement states the products were distributed nationwide through select retail, online via trueseamoss.com, and other distribution channels. The recall includes multiple listed flavors with associated UPC codes, including:
- Mango (UPC 5065006235875)
- Pineapple (UPC 5065006235288)
- Wildcrafted (UPC 5065006235073)
- Apple and Cinnamon (UPC 5065006235776)
- Elderberry (UPC 5065006235189)
- Passion Fruit (UPC 5061033691882)
- Blue Spirulina and Raspberry (UPC 5065006235813)
- Strawberry (UPC 5065006235271)
- Cherry (UPC 5061033691264)
- Mango and Pineapple (UPC 5065006235301)
- 5 Blends in 1 (UPC 5061033690052)
- Soursop (UPC 5061033691875)
- Lemon Pie (UPC 5061033691271)
- Orange (UPC 5061033692926)
Injuries & Potential Health Effects
FDA’s posted announcement states no illnesses or adverse health events had been reported at the time of the recall. The health concern identified in the notice is the potential for microbial growth, including organisms that can produce toxins associated with botulism. Symptoms described in the recall notice may include general weakness, dizziness, double vision, difficulty speaking or swallowing, and, in severe cases, difficulty breathing or muscle weakness. Anyone experiencing symptoms after consuming the product should seek medical attention immediately, especially where breathing or swallowing is affected.
Do You Qualify for a True Sea Moss Gel Recall Lawsuit?
You may qualify to pursue a True Sea Moss Gel Recall Lawsuit if one or more of the following applies:
- You purchased True Sea Moss Sea Moss Gel Superfood in a 16 FL OZ (473 mL) glass jar manufactured prior to January 9, 2026 (check the MFD on the lid).
- You consumed the product and developed symptoms consistent with the recall notice’s described botulism-related risk, requiring medical evaluation or treatment.
- You incurred expenses tied to the recall, such as medical bills, lost time from work, or other documented losses after a suspected exposure event.
- You have proof connecting the product to the exposure (receipt, packaging, jar lid MFD photo, UPC, or other documentation).
Evidence You Should Gather
- Photos of the jar and lid showing the MFD (MM/YYYY) and any identifying labels.
- Receipts or order confirmations (including online purchases via trueseamoss.com or other channels).
- Medical records documenting symptoms, diagnosis, treatment, and timelines of illness onset.
- Proof of out-of-pocket costs, including travel to care, pharmacy costs, and missed work documentation.
- Any communications with the retailer or company about return/disposal instructions.
Damages You Can Recover
Potential damages depend on the facts and applicable state law, but can include:
- Medical expenses (ER visits, hospitalization, diagnostic testing, specialist care, follow-up).
- Lost wages or lost earning capacity tied to illness and recovery time.
- Pain and suffering and emotional distress associated with severe foodborne illness concerns.
- Out-of-pocket costs related to treatment and recovery.
Legal Theories & Liability Grounds
Food recall claims commonly involve product liability and negligence frameworks. Based on the recall notice’s stated issue, potential legal theories may include:
- Negligence: alleged failure to implement required controls and records for pH-controlled food safety in a way that prevented microbial-risk conditions.
- Strict product liability: claims that a food product entered commerce in a condition that posed an unreasonable risk of harm.
- Failure to warn: claims that warnings and instructions were insufficient to prevent injury prior to the recall notice.
Statute of Limitations & Timing
Time limits for filing a food-related injury claim vary by state and can depend on the date of injury or the date an illness was discovered. Preserving the jar, lid, MFD information, and purchase evidence can be important when evaluating legal options. The recall notice directs consumers to discontinue use and follow the place-of-purchase instructions for return or disposal, so consider documenting the product thoroughly before disposing of it.
Frequently Asked Questions
- What should I do if I still have True Sea Moss Gel at home?
Discontinue use and follow the place-of-purchase instructions for product return or disposal. - How can I identify recalled product?
The recall applies to all flavors and batch numbers of True Sea Moss Sea Moss Gel Superfood packaged in 16 FL OZ (473 mL) glass jars manufactured prior to January 9, 2026, with MFD shown on the lid in MM/YYYY format, and the recall notice lists specific UPCs by flavor. - How do I contact the company?
The recall notice lists: support@divafam.com and (818) 751-3882, Monday through Friday, 9:00 a.m. to 5:00 p.m. PT.
Why You Should Act Now
This recall involves a potential botulism-related food safety risk tied to missing regulatory authorization and temperature monitoring records for a pH-controlled food product. If you purchased True Sea Moss Sea Moss Gel Superfood, stop using it and follow the return or disposal instructions from the place of purchase. If you became ill or incurred losses after consuming the product, a legal review can help determine whether a True Sea Moss Gel Recall Lawsuit is appropriate and what documentation is needed to support a claim.
References
- https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/diva-fam-inc-announces-voluntary-recall-sea-moss-gel-superfood-products-due-possible-health-risk