, Best Choice Mountain Trail Mix, Best By/Date Code: 3/14/2017.
Recalling firm: Treehouse Foods
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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041498148447, 070038614142, 075450016796, 075450040739FDA code information
Best By/Date Code: 3/14/2017, 4/4/2017, 4/5/2017, 4/15/2017, 4/26/2017, 3/23/2017.
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Full FDA record and distribution details
Original product description
UPC 070038614142, Best Choice Mountain Trail Mix, Best By/Date Code: 3/14/2017. UPC 041498148447, Southern Grove Mountain Trail Mix, Best by Date Code: 4/4/2017, 4/26/2017. UPC 075450016796, Hy-Vee Mountain Mix Trail Mix, Best By/Date Code: 4/5/2017, 4/15/2017. UPC 075450040739, Hy-Vee Mountain Trail Mix, Best By/Date Code: 3/23/2017.
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 041498148447 | 8614142, Best Choice Mountain Trail Mix, Best By/Date Code: 3/14/2017. UPC 041498148447, Southern Grove Mountain Trail Mix, Best by Date Code: 4/4/2017, 4/26/2017. UPC 075450016796, Hy-Vee Mountain Mix T |
| UPC | 070038614142 | UPC 070038614142, Best Choice Mountain Trail Mix, Best By/Date Code: 3/14/2017. UPC 041498148447, Southern Grove Mountain Trail Mix |
| UPC | 075450016796 | uthern Grove Mountain Trail Mix, Best by Date Code: 4/4/2017, 4/26/2017. UPC 075450016796, Hy-Vee Mountain Mix Trail Mix, Best By/Date Code: 4/5/2017, 4/15/2017. UPC 075450040739, Hy-Vee Mountain Trail M |
| UPC | 075450040739 | Hy-Vee Mountain Mix Trail Mix, Best By/Date Code: 4/5/2017, 4/15/2017. UPC 075450040739, Hy-Vee Mountain Trail Mix, Best By/Date Code: 3/23/2017. |
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-2411-2016
- 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.
Data updated September 16, 2026. View official FDA data ↗
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