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Policy version 2026-07-21, effective July 21, 2026.
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 Terminated Historical recordClass II
Responsible company: Friendly Fruit Market dba Sid Wainer & Son
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical recordClass II
FDA Recall United States Terminated Historical 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.
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.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
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.
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.
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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