NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED ORGANIC CHIA SEED (SALVIA HISPANICA).
Summary
The FDA issued a Class I for NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) INGREDIENTS: CERTIFIED by Navitas, LLC.. Reason: Potential contamination with Salmonella..
Details
Source
Food Recall
External ID
H-0533-2026
Action Date
2026-03-04
Status
Ongoing
Category
food
Product Description
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
Lot/Code Info: 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
Quantity Affected: 114,432 units (9,536 cases ; 12 units/case)
Reason for Recall
Potential contamination with Salmonella.
Distribution
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
Type: Voluntary: Firm initiated
Recall Initiated: 2026-01-23
Company
San Rafael, CA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 27 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Navitas, LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Navitas, LLC. have FDA actions?
This is the only FDA action we have on record for Navitas, LLC. in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0533-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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