FDA Recall United States Ongoing 2026 recordClass I
Navitas, LLC.
- Product
- NAVITAS ORGANICS ORGANIC CHIA SEEDS NET WT 8 OZ (227g) IN…
- Published
- March 4, 2026
- Distribution
- U.S. Distribution: CA, CO, CT, FL, GA, I…
Navitas, LLC. Recall: Firm was notified by manufacturer that four varieties of their Superfood bars were made using sunflower seeds under recall for Listeria Monocytogenes.
United States
TerminatedClass I
- Company
- Navitas, LLC.
- Product
- Navitas Naturals Superfood Cacao bar: Tart Cranberry, Cacao…
- Recall date
- June 2, 2016
- Terminated
- October 19, 2016
- Source
- FDA
Reason for recall
Firm was notified by manufacturer that four varieties of their Superfood bars were made using sunflower seeds under recall for Listeria Monocytogenes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Navitas Naturals Superfood Cacao bar: Tart Cranberry, Cacao, Nut Bar Net WT. 1.4 oz/40 G. Gluten free. Ingredients: Distributed by Navitas Naturals, Novato, CA. | Not published in this source record | Not published in this source record | Not published in this source record |
Distribution
- NY
- NH
- CT
- PA
- GA
- FL
- IN
- IA
- WI
- TX
- CA
- WA
- CO
- OR
- DC
- ME
- MD
- UT
- SC
- MI
- and one consignee in Canada
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1686-2016
- Status
- Terminated
- Classification
- Class I
- Company
- Navitas, LLC.
- Product description
- Navitas Naturals Superfood Cacao bar: Tart Cranberry, Cacao, Nut Bar Net WT. 1.4 oz/40 G. Gluten free. Ingredients: Distributed by Navitas Naturals, Novato, CA.
- Quantity
- Not published in this source record
- Reason
- Firm was notified by manufacturer that four varieties of their Superfood bars were made using sunflower seeds under recall for Listeria Monocytogenes.
- Recall initiation date
- June 2, 2016
- Report date
- July 27, 2016
- Classification date
- Not published in this source record
- Termination date
- October 19, 2016
- Distribution pattern
- NY, NH, CT, PA, GA, FL, IN, IA, WI, TX, CA, WA, CO, OR, DC, ME, MD, UT, SC, MI, and one consignee in Canada
- UPC, lot, and code information
- Not published in this source record
- Voluntary or mandated
- Not published in this source record
- Initial notification method
- Not published in this source record
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: Navitas, LLC.
Other recalls from Navitas, LLC.
FDA Recall United States Terminated Historical recordClass I
Navitas, LLC.
- Product
- Navitas Naturals Superfood Hemp bar: Creamy Peanut, Hemp, N…
- Published
- July 27, 2016
- Distribution
- NY, NH, CT, PA, GA, FL, IN, IA, WI, TX,…
FDA Recall United States Terminated Historical recordClass I
Navitas, LLC.
- Product
- Navitas Naturals Superfood Maca bar: Sweet Maple, Maca, Nut…
- Published
- July 27, 2016
- Distribution
- NY, NH, CT, PA, GA, FL, IN, IA, WI, TX,…
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| New York | 1 |
| New Hampshire | 1 |
| Connecticut | 1 |
| Pennsylvania | 1 |
| Georgia | 1 |
| Florida | 1 |
| Indiana | 1 |
| Iowa | 1 |
| Wisconsin | 1 |
| Texas | 1 |
| California | 1 |
| Washington | 1 |
| Colorado | 1 |
| Oregon | 1 |
| District of Columbia | 1 |
| Maine | 1 |
| Maryland | 1 |
| Utah | 1 |
| South Carolina | 1 |
| Michigan | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class I mean?
A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
