---
title: "Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Elderberry- UP... — FDA record H-0471-2026 | Is It on Recall"
description: "potential Clostridium botulinum contamination"
url: https://isitonrecall.com/recall/fda-food-h-0471-2026-sea-moss-gel-superfood-16-fl-oz-glass-jar-sold-individually-elderberry-upc-5065006235189/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Elderberry- UPC# 5065006235189 — FDA record H-0471-2026

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jan 9, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Sea Moss Gel Superfood; 16 FL OZ; Glass jar sold individually. Elderberry- UPC# 5065006235189
- **Reason**: potential Clostridium botulinum contamination
- **Classification**: Class II
- **Recalling firm**: Diva Fam Inc
- **Quantity**: 5,438,998 units across all recalled products
- **Agency-reported status**: Terminated
- **Source record identifier**: H-0471-2026

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0471-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Lot Codes: Elderberry- E1001, E1002, E1003, E1004, E1005, E1006, E1007, E1008, E1009, E1010, E1011, E1012, E1013, E1014, E1015, E1016, E1017, E1018, E1019, E2001, E2002, E2003, E2004, E2005, E2006, E250102, E250116, E250117, E250207, E250216, E250219, E250227, E250304, E250307, E250309, E250317, E250321, E250326, E250403, E250406, E250410, E250419, E250422, E250429, E250430, E250502, E250504, E250511, E250518, E250528, E250602, E250609, E250615 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Product is distributed nationwide through 31 different retail customers and direct to consumers through online sales.

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Feb 11, 2026
- **Recall initiation date**: Jan 9, 2026
- **Center classification date**: Feb 4, 2026
- **Termination date**: Aug 11, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-0471-2026%22)

## Related records

[Other food records](https://isitonrecall.com/category/other-food/) [Diva Fam Inc records](https://isitonrecall.com/brand/diva-fam-inc/)
