FDA Recall United States Terminated Historical recordClass I
Figi's, Inc
- Product
- Snack Shoppe, 16 OZ Hot & Spicy Cajun Snack Mix in a foil ba…
- Published
- September 28, 2016
- Distribution
- CO, FL, GA, IL, KY, LA, MI, MN, NJ, NY,…
Figi's, Inc Recall: Figi's Companies, Inc is recalling 2 products that are related to the SunOpta sunflower kernel recall, because they have the potential to be contaminated with Listeria monocytogenes.
United States
TerminatedClass I
- Company
- Figi's, Inc
- Product
- Figi's Gifts in Good Taste, 16 OZ (453.60 g) Nature's Mix i…
- Recall date
- June 24, 2016
- Terminated
- March 30, 2017
- Source
- FDA
Reason for recall
Figi's Companies, Inc is recalling 2 products that are related to the SunOpta sunflower kernel recall, because they have the potential to be contaminated with Listeria monocytogenes.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Figi's Gifts in Good Taste, 16 OZ (453.60 g) Nature's Mix in a plastic bag that is a red circular tin container. Nature's Mix is packaged in a plastic bulk bag with approximately 8-12 ounces o product. | Not published in this source record | 2212.75 lbs | not available |
Distribution
- CO
- FL
- GA
- IL
- KY
- LA
- MI
- MN
- NJ
- NY
- NC
- OH
- OR
- PA
- SC
- TX
- VA
- WV.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-2277-2016
- Event ID
- 74572
- Status
- Terminated
- Classification
- Class I
- Company
- Figi's, Inc
- Product description
- Figi's Gifts in Good Taste, 16 OZ (453.60 g) Nature's Mix in a plastic bag that is a red circular tin container. Nature's Mix is packaged in a plastic bulk bag with approximately 8-12 ounces o product.
- Quantity
- 2212.75 lbs
- Reason
- Figi's Companies, Inc is recalling 2 products that are related to the SunOpta sunflower kernel recall, because they have the potential to be contaminated with Listeria monocytogenes.
- Recall initiation date
- June 24, 2016
- Report date
- September 28, 2016
- Classification date
- Not published in this source record
- Termination date
- March 30, 2017
- Distribution pattern
- CO, FL, GA, IL, KY, LA, MI, MN, NJ, NY, NC, OH, OR, PA, SC, TX, VA, WV.
- UPC, lot, and code information
- not available
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 74572 with 1 other product entry in Public Health Trace.
Responsible company: Figi's, Inc
Other recalls from Figi's, Inc
FDA Recall United States Terminated Historical recordClass II
Figi's, Inc
- Product
- Dark Chocolate covered Gingersnaps. Packaged as follows: 1…
- Published
- January 10, 2018
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Figi's, Inc
- Product
- Snack Shoppe, 16 OZ Hot & Spicy Cajun Snack Mix in a foil ba…
- Published
- September 28, 2016
- Distribution
- CO, FL, GA, IL, KY, LA, MI, MN, NJ, NY,…
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 |
|---|---|
| Colorado | 1 |
| Florida | 1 |
| Georgia | 1 |
| Illinois | 1 |
| Kentucky | 1 |
| Louisiana | 1 |
| Michigan | 1 |
| Minnesota | 1 |
| New Jersey | 1 |
| New York | 1 |
| North Carolina | 1 |
| Ohio | 1 |
| Oregon | 1 |
| Pennsylvania | 1 |
| South Carolina | 1 |
| Texas | 1 |
| Virginia | 1 |
| West Virginia | 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.
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