United States
TerminatedClass II
Products were labeled with incorrect ingredient listing. The ingredients listed on the label include multiple allergens (almonds, cashews, coconut, hazelnuts, pecans, walnuts, peanuts). Label lists allergens that are not actually in the product. Allergens actually present in the product are: peanuts, almonds, cashews, coconut, hazelnuts, walnuts.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Jansal Valley brand Energize Snack Mix NET WT 5 OZ (142 G) in plastic clamshells, Ingredients: apricots, almonds, banana chips, coconut, cashews, dates, raisins, hazelnuts, pecans, pepitas, walnuts, papaya, pineapple. Contains: almonds, cashews, coconut, hazelnuts, pecans, walnuts.isins, vegetable oil). Contains: peanuts, almonds, cashews, coconut, hazelnuts, walnuts. This product is packaged in a facility that also packages tree nuts, peanuts, wheat, soy and dairy Distributed Exclusively by Sid Wainer & Son New Bedford, MA 02746 USA JANSALVALLEY.COM UPC: 708152329412 | 708152329412 | 562 clamshells | Lots: 12303196, 11582, 10909, 10467 Best By Dates: 7/11/2019, 8/6/2019, 8/11/2019, 8/20/2019, 9/4/2019, 9/14/2019, 10/4/2019, 10/11/2019, 10/23/2019, 11/06/2019, 11/08/2019, 11/10/2019, 11/20/2019, 11/21/2019, 1/1/2020, 1/29/2020, 2/26/2020 |
This recall shares FDA event ID 83922 with 1 other product entry in Public Health Trace.
FDA Recall United States TerminatedTerminated: January 13, 2020Historical recordClass II
Responsible company: Friendly Fruit Market dba Sid Wainer & Son
FDA Recall United States TerminatedTerminated: January 13, 2020Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2019Historical recordClass II
FDA Recall United States TerminatedTerminated: March 21, 2019Historical recordClass II
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 |
|---|---|
| Massachusetts | 1 |
| Maine | 1 |
| Connecticut | 1 |
| New York | 1 |
| Vermont | 1 |
| Virginia | 1 |
| Rhode Island | 1 |
| District of Columbia | 1 |
| Florida | 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.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.
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View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
FDA classifies this recall as Class II. See how to read an FDA recall record (linked above) for what each classification level means.
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.
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This record is preserved as published by FDA, as of January 13, 2020.
Status as reported: Terminated.
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