NSI Group LLC Recall: Product testing was found positive for Salmonella.
United States
TerminatedClass I
- Company
- NSI Group LLC
- Product
- Volupta Organic Black Chia Seeds 64 oz. Best By: 10/31/2025…
- Recall date
- March 23, 2023
- Terminated
- May 23, 2023
- Source
- FDA
Reason for recall
Product testing was found positive for Salmonella.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Volupta Organic Black Chia Seeds 64 oz. Best By: 10/31/2025 Stand up pouch. Product of Paraguay | Not published in this source record | 1,351 pouches | Lot 23068 - C023 FG00323 |
Distribution
- U.S. distribution to one Costco retail location in San Diego
- CA
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-0734-2023
- Event ID
- 91960
- Status
- Terminated
- Classification
- Class I
- Company
- NSI Group LLC
- Product description
- Volupta Organic Black Chia Seeds 64 oz. Best By: 10/31/2025 Stand up pouch. Product of Paraguay
- Quantity
- 1,351 pouches
- Reason
- Product testing was found positive for Salmonella.
- Recall initiation date
- March 23, 2023
- Report date
- April 26, 2023
- Classification date
- Not published in this source record
- Termination date
- May 23, 2023
- Distribution pattern
- U.S. distribution to one Costco retail location in San Diego, CA
- UPC, lot, and code information
- Lot 23068 - C023 FG00323
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Letter
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Responsible company: NSI Group LLC
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 |
|---|---|
| California | 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.
