Diva Fam Inc. announced a voluntary recall of all lots and flavors of its Sea Moss Gel Superfood products on Jan. 9, 2026, citing lack of required regulatory authorization and missing temperature monitoring records for pH-controlled food products. The Los Angeles-based company initiated the recall after identifying compliance deficiencies that could pose potential health risks to consumers.
The recall affects all Sea Moss Gel Superfood products manufactured and distributed by Diva Fam, regardless of lot number or flavor variety. The company cited two primary regulatory violations that prompted the voluntary action: absence of required FDA regulatory authorization and inadequate temperature monitoring records for products classified as pH-controlled foods.
Sea moss, scientifically known as Chondrus crispus, has gained popularity in recent years as a superfood supplement marketed for its purported health benefits. The gel form of the product requires specific handling and storage protocols to ensure food safety, particularly regarding temperature control and pH monitoring.
The FDA classifies certain food products as pH-controlled foods when their safety depends on maintaining specific acidity levels. These products require manufacturers to establish and maintain detailed monitoring systems to prevent the growth of harmful bacteria, particularly Clostridium botulinum, which can cause botulism. The lack of proper temperature monitoring records indicates potential gaps in the company's food safety management system.
Regulatory authorization requirements exist to ensure that food manufacturers meet established safety standards before bringing products to market. The absence of such authorization suggests that Diva Fam may have been operating without proper FDA clearance for its Sea Moss Gel Superfood line.
The voluntary nature of the recall indicates that Diva Fam proactively identified the compliance issues and took corrective action before receiving a formal FDA mandate. Companies that voluntarily recall products often receive more favorable regulatory treatment than those subject to mandatory recalls initiated by federal agencies.
Consumers who have purchased Sea Moss Gel Superfood products from Diva Fam are advised to discontinue use immediately and dispose of the products safely. The company has not yet announced specific procedures for consumer refunds or exchanges, though such information typically becomes available as recall procedures are implemented.
The recall highlights ongoing challenges in the rapidly expanding superfood and dietary supplement industry, where products often enter the market with limited regulatory oversight. Sea moss products, in particular, have proliferated across various retail channels, including online marketplaces, health food stores, and direct-to-consumer sales platforms.
Food safety experts note that pH-controlled products require sophisticated manufacturing processes and quality control systems to ensure consumer safety. The monitoring requirements serve as critical control points in preventing foodborne illness outbreaks that could result from improper handling or storage.
The FDA has increased scrutiny of superfood products in recent years, particularly those making health claims or requiring special handling procedures. The agency's enforcement actions have targeted companies that market products without proper authorization or fail to maintain adequate safety records.
Diva Fam's recall comes amid broader industry discussions about regulatory frameworks for emerging food products. The superfood market has experienced rapid growth, with sea moss products representing a significant segment driven by social media marketing and celebrity endorsements.
The company has not disclosed the volume of products affected by the recall or the geographic distribution of the Sea Moss Gel Superfood line. Such information typically emerges during the recall investigation process as the FDA works with the manufacturer to assess the scope of potential consumer exposure.
Regulatory compliance in the food industry requires manufacturers to establish comprehensive quality assurance programs that include proper documentation, temperature monitoring, and safety testing. The violations identified in Diva Fam's case suggest potential systemic issues in the company's manufacturing or quality control processes.
The recall announcement serves as a reminder to consumers about the importance of purchasing food products from manufacturers that maintain proper regulatory compliance. The FDA recommends that consumers verify that dietary supplements and specialty food products come from reputable sources with established quality control systems.
Industry observers expect the FDA to conduct a thorough investigation of Diva Fam's manufacturing processes and regulatory compliance history. Such investigations typically examine production facilities, quality control documentation, and distribution records to assess the full scope of potential violations.
The outcome of this recall may influence how the FDA approaches oversight of similar products in the superfood category. Regulatory agencies often use individual cases to establish precedents for industry-wide enforcement actions and compliance expectations.