Diva Fam recalls 16 fl oz Sea Moss Gel Superfood (glass jar) due to potential Clostridium botulinum contamination. Affected lots include Strawberry- S1001 to S250615. Consumers should stop using immediately.
potential Clostridium botulinum contamination
Diva Fam is recalling 16 fl oz Sea Moss Gel Superfood in glass jars sold with a strawberry flavor. The product may contain Clostridium botulinum, a bacteria that can cause botulism illness, which is serious and potentially life-threatening.
Clostridium botulinum is a bacterium that produces a toxin causing botulism, a serious illness that can lead to paralysis and even death if not treated promptly. The contamination in this product could occur during manufacturing or storage, especially if the product was not properly sealed.
Anyone who purchased the Sea Moss Gel Superfood in glass jars with the strawberry flavor and the listed lot codes. People who consume the product may be at risk of botulism.
Check for glass jars labeled 'Sea Moss Gel Superfood' with a strawberry flavor and the UPC number 5065006235271. The affected lots are identified by the codes starting with 'Strawberry-' followed by numbers like S1001 to S250615.
Discard the product if you have the affected lot codes listed in the recall notice.
No, the product may contain Clostridium botulinum, which can cause serious illness. Do not consume the affected products.
The affected lot codes are Strawberry- S1001 to S250615 as listed in the recall notice.
Check the product label for the UPC number 5065006235271 and the lot codes starting with 'Strawberry-' followed by numbers like S1001 to S250615.
We’ve drafted a message you can send Diva Fam to request your refund or repair — edit it as you like.
Subject: Recall H-0474-2026 — Diva Fam Diva Fam Hello, I own a Diva Fam that is covered by recall H-0474-2026 from Diva Fam. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
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