Class IOngoingVoluntary: Firm initiated
Navitas, LLC.: food recall H-0533-2026
Navitas, LLC. of San Rafael, CA recalled NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED ORGANIC CHIA SEED (SALVIA HISPANICA).… Reason: Potential contamination with Salmonella. The FDA listed it as Class I in its Enforcement Report dated Mar 4, 2026; distribution: California, Colorado, Connecticut, Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Massachusetts, Maryland, Mississippi, North Carolina, New Hampshire, New Jersey, New Mexico, Nevada, New York, Ohio, Oregon, Pennsylvania, Tennessee, Texas, Vermont, Washington, Wisconsin.
Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED ORGANIC CHIA SEED (SALVIA HISPANICA). Product of Mexico/Argentina/Paraguay. Distributed by Navitas Organics Novato, CA USA 94949 UPC: 858847000284
- Product quantity
- 114,432 units (9,536 cases ; 12 units/case)
- Reason for recall
- Potential contamination with Salmonella.
- Codes, lots and dates on the package
- W31025283 - Best If Used By: End APR 2027 W31025286 - Best If Used By: End APR 2027 W31025287 - Best If Used By: End APR 2027 W31025311 - Best If Used By: End MAY 2027 W31025314 - Best If Used By: End MAY 2027 W31025315 - Best If Used By: End MAY 2027 W31025316 - Best If Used By: End MAY 2027 W31025317 - Best If Used By: End MAY 2027
- Distribution pattern
- U.S. Distribution: CA, CO, CT, FL, GA, IA, IL, IN, KY, MA, MD, MS, NC, NH, NJ, NM, NV, NY, OH, OR, PA, TN, TX, VT, WA, WI. Foreign Distribution: None
- Recalling firm
- Navitas, LLC., San Rafael, CA
- Classification
- Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Jan 23, 2026 |
| Classified by the FDA | Feb 26, 2026 |
| Published in the Enforcement Report | Mar 4, 2026 |
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0533-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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