Class ITerminated in FDA datasetRecall initiated May 3, 2016

, Southern Grove Oven Roasted Almonds with Sea Salt, Best By/Date Code: 3/16/2017.

Recalling firm: Treehouse Foods

Why it was recalled

TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Aug 15, 2017.

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Compare the exact product and package details with the label you have.

ProductUPC 041498132248, Southern Grove Oven Roasted Almonds with Sea Salt, Best By/Date Code: 3/16/2017. UPC 041498132248, Southern Grove Dry Roasted Sea Salt Almond, Best By/Date Code 3/4/2017. UPC 071725728791, Nature's Harvest Almond Dry Roasted Sea Salted, Best By/Date Code 3/16/2017.
UPC041498132248, 071725728791

FDA code information

Best By/Date Code: 3/16/2017, 3/4/2017.

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Full FDA record and distribution details

Original product description

UPC 041498132248, Southern Grove Oven Roasted Almonds with Sea Salt, Best By/Date Code: 3/16/2017. UPC 041498132248, Southern Grove Dry Roasted Sea Salt Almond, Best By/Date Code 3/4/2017. UPC 071725728791, Nature's Harvest Almond Dry Roasted Sea Salted, Best By/Date Code 3/16/2017.

Extracted codes and context

TypeCode / valueContext
UPC041498132248UPC 041498132248, Southern Grove Oven Roasted Almonds with Sea Salt, Best By/Date Code: 3/16/2017. UPC 041498132248, Southern Grove
UPC041498132248 Grove Oven Roasted Almonds with Sea Salt, Best By/Date Code: 3/16/2017. UPC 041498132248, Southern Grove Dry Roasted Sea Salt Almond, Best By/Date Code 3/4/2017. UPC 071725728791, Nature's Harvest Almond
UPC071725728791outhern Grove Dry Roasted Sea Salt Almond, Best By/Date Code 3/4/2017. UPC 071725728791, Nature's Harvest Almond Dry Roasted Sea Salted, Best By/Date Code 3/16/2017.

Original FDA recall reason

TreeHouse Foods is recalling products that may be impacted by sunflower seeds contaminated with Listeria monocytogenes.

Recall details

Recall number
F-2430-2016
Event ID
74041
FDA status
Terminated
Initiated
May 3, 2016
Reported
Oct 12, 2016
Classified
Sep 30, 2016
Terminated
Aug 15, 2017
Quantity
92,865 cases for all products
Location
Oak Brook, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

US: AL, AZ, AR, CA, CO, CT, FL, IL, IN, IA, KS,KY, LA, ME, MD, MA, MI, MN, MS, MO, NE, NV, NM, NY, NC,ND, OH, OK, OR, PA,SC, TN, TX, UT, VA, WA, WI, WY. OUS: HONDURAS, NICARAGUA, CHILE.

FDA source record · F-2430-2016

Data updated September 16, 2026. View official FDA data ↗

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